|
Variants on interaction residues
|
|
KEGG pathway |
Name |
|
hsa00010
|
Glycolysis / Gluconeogenesis
|
|
dbSNP |
Type |
Disease name |
|
-
|
Disease |
Maturity-onset diabetes of the young 2 (MODY2) [MIM:125851] |
|
-
|
Disease |
Pyruvate kinase deficiency of red cells (PKRD) [MIM:266200] |
|
-
|
Disease |
Phosphoglycerate kinase 1 deficiency (PGK1D) [MIM:300653] |
|
-
|
Disease |
Pyruvate dehydrogenase E1-alpha deficiency (PDHAD) [MIM:312170] |
|
-
|
Disease |
Diabetes mellitus, permanent neonatal (PNDM) [MIM:606176] |
|
-
|
Disease |
Congenital disorder of glycosylation 1T (CDG1T) [MIM:614921] |
|
-
|
Disease |
Microphthalmia, isolated, 8 (MCOP8) [MIM:615113] |
|
rs1041969
|
Polymorphism |
- |
|
rs104894009
|
Disease |
Maturity-onset diabetes of the young 2 (MODY2) [MIM:125851] |
|
rs104894015
|
Disease |
Familial hyperinsulinemic hypoglycemia 3 (HHF3) [MIM:602485] |
|
rs1131691416
|
Disease |
Maturity-onset diabetes of the young 2 (MODY2) [MIM:125851] |
|
rs1167329263
|
Disease |
Pyruvate kinase deficiency of red cells (PKRD) [MIM:266200] |
|
rs121912707
|
Disease |
Pyridoxine-dependent epilepsy (PDE) [MIM:266100] |
|
rs121912711
|
Disease |
Pyridoxine-dependent epilepsy (PDE) [MIM:266100] |
|
rs121964925
|
Disease |
Erythrocytosis, familial, 8 (ECYT8) [MIM:222800] |
|
rs121964988
|
Disease |
Dihydrolipoamide dehydrogenase deficiency (DLDD) [MIM:246900] |
|
rs121964991
|
Disease |
Dihydrolipoamide dehydrogenase deficiency (DLDD) [MIM:246900] |
|
rs121964993
|
Disease |
Dihydrolipoamide dehydrogenase deficiency (DLDD) [MIM:246900] |
|
rs1229984
|
Polymorphism |
- |
|
rs1286804191
|
Disease |
Diabetes mellitus, permanent neonatal (PNDM) [MIM:606176] |
|
rs1320810473
|
Disease |
Congenital disorder of glycosylation 1T (CDG1T) [MIM:614921] |
|
rs1375656631
|
Disease |
Maturity-onset diabetes of the young 2 (MODY2) [MIM:125851] |
|
rs137852530
|
Polymorphism |
- |
|
rs137852533
|
Disease |
Phosphoglycerate kinase 1 deficiency (PGK1D) [MIM:300653] |
|
rs137853258
|
Disease |
Pyruvate dehydrogenase E1-alpha deficiency (PDHAD) [MIM:312170] |
|
rs1441649062
|
Disease |
Maturity-onset diabetes of the young 2 (MODY2) [MIM:125851] |
|
rs147065275
|
Disease |
Maturity-onset diabetes of the young 2 (MODY2) [MIM:125851] |
|
rs148311934
|
Disease |
Maturity-onset diabetes of the young 2 (MODY2) [MIM:125851] |
|
rs1554335135
|
Disease |
Maturity-onset diabetes of the young 2 (MODY2) [MIM:125851] |
|
rs17853396
|
Polymorphism |
- |
|
rs193922272
|
Disease |
Maturity-onset diabetes of the young 2 (MODY2) [MIM:125851] |
|
rs193922282
|
Disease |
Diabetes mellitus, permanent neonatal (PNDM) [MIM:606176] |
|
rs193922297
|
Disease |
Maturity-onset diabetes of the young 2 (MODY2) [MIM:125851] |
|
rs193922311
|
Disease |
Maturity-onset diabetes of the young 2 (MODY2) [MIM:125851] |
|
rs2066702
|
Polymorphism |
- |
|
rs28359542
|
Polymorphism |
- |
|
rs28383586
|
Polymorphism |
- |
|
rs28730628
|
Polymorphism |
- |
|
rs35385902
|
Polymorphism |
- |
|
rs398122379
|
Disease |
Hexokinase deficiency (HK deficiency) [MIM:235700] |
|
rs671
|
Polymorphism |
- |
|
rs747097960
|
Disease |
Pyruvate kinase deficiency of red cells (PKRD) [MIM:266200] |
|
rs751972865
|
Disease |
Erythrocytosis, familial, 8 (ECYT8) [MIM:222800] |
|
rs758737171
|
Disease |
Familial hyperinsulinemic hypoglycemia 3 (HHF3) [MIM:602485] |
|
rs769268803
|
Disease |
Maturity-onset diabetes of the young 2 (MODY2) [MIM:125851] |
|
rs769724893
|
Polymorphism |
- |
|
rs777954556
|
Disease |
Lactate dehydrogenase B deficiency (LDHBD) [MIM:614128] |
|
rs80356655
|
Disease |
Maturity-onset diabetes of the young 2 (MODY2) [MIM:125851] |
|
rs80356655
|
Disease |
Diabetes mellitus, permanent neonatal (PNDM) [MIM:606176] |
|
rs981505482
|
Disease |
Pyruvate kinase deficiency of red cells (PKRD) [MIM:266200] |
|
hsa00020
|
Citrate cycle (TCA cycle)
|
|
dbSNP |
Type |
Disease name |
|
-
|
Disease |
Pyruvate dehydrogenase E1-alpha deficiency (PDHAD) [MIM:312170] |
|
rs1057519906
|
Polymorphism |
- |
|
rs121913499
|
Unclassified |
A glioma sample |
|
rs121913502
|
Disease |
D-2-hydroxyglutaric aciduria 2 (D2HGA2) [MIM:613657] |
|
rs121964988
|
Disease |
Dihydrolipoamide dehydrogenase deficiency (DLDD) [MIM:246900] |
|
rs121964991
|
Disease |
Dihydrolipoamide dehydrogenase deficiency (DLDD) [MIM:246900] |
|
rs121964993
|
Disease |
Dihydrolipoamide dehydrogenase deficiency (DLDD) [MIM:246900] |
|
rs137853258
|
Disease |
Pyruvate dehydrogenase E1-alpha deficiency (PDHAD) [MIM:312170] |
|
rs28359542
|
Polymorphism |
- |
|
rs28383586
|
Polymorphism |
- |
|
rs28940589
|
Disease |
Pyruvate carboxylase deficiency (PC deficiency) [MIM:266150] |
|
rs28940590
|
Disease |
Pyruvate carboxylase deficiency (PC deficiency) [MIM:266150] |
|
rs782308462
|
Disease |
Epileptic encephalopathy, early infantile, 51 (EIEE51) [MIM:617339] |
|
hsa00030
|
Pentose phosphate pathway
|
|
dbSNP |
Type |
Disease name |
|
-
|
Disease |
Anemia, non-spherocytic hemolytic, due to G6PD deficiency (NSHA) [MIM:300908] |
|
-
|
Unclassified |
Hemolytic anemia, non-spherocytic, due to glucose phosphate isomerase deficiency (HA-GPID) [MIM:613470] |
|
rs1250029517
|
Disease |
Hemolytic anemia, non-spherocytic, due to glucose phosphate isomerase deficiency (HA-GPID) [MIM:613470] |
|
rs137852316
|
Disease |
Anemia, non-spherocytic hemolytic, due to G6PD deficiency (NSHA) [MIM:300908] |
|
rs137852325
|
Disease |
Anemia, non-spherocytic hemolytic, due to G6PD deficiency (NSHA) [MIM:300908] |
|
rs137852329
|
Disease |
Anemia, non-spherocytic hemolytic, due to G6PD deficiency (NSHA) [MIM:300908] |
|
rs137852349
|
Disease |
Anemia, non-spherocytic hemolytic, due to G6PD deficiency (NSHA) [MIM:300908] |
|
rs137852543
|
Disease |
Phosphoribosylpyrophosphate synthetase superactivity (PRPS1 superactivity) [MIM:300661] |
|
rs137852545
|
Disease |
Phosphoribosylpyrophosphate synthetase superactivity (PRPS1 superactivity) [MIM:300661] |
|
rs137853582
|
Disease |
Hemolytic anemia, non-spherocytic, due to glucose phosphate isomerase deficiency (HA-GPID) [MIM:613470] |
|
rs138207257
|
Disease |
Hyperoxaluria primary 3 (HP3) [MIM:613616] |
|
rs139382538
|
Disease |
Hemolytic anemia, non-spherocytic, due to glucose phosphate isomerase deficiency (HA-GPID) [MIM:613470] |
|
rs76645461
|
Disease |
Anemia, non-spherocytic hemolytic, due to G6PD deficiency (NSHA) [MIM:300908] |
|
rs78478128
|
Disease |
Anemia, non-spherocytic hemolytic, due to G6PD deficiency (NSHA) [MIM:300908] |
|
rs80338675
|
Disease |
ARTS syndrome (ARTS) [MIM:301835] |
|
hsa00040
|
Pentose and glucuronate interconversions
|
|
dbSNP |
Type |
Disease name |
|
-
|
Disease |
46,XY sex reversal 8 (SRXY8) [MIM:614279] |
|
rs121912707
|
Disease |
Pyridoxine-dependent epilepsy (PDE) [MIM:266100] |
|
rs121912711
|
Disease |
Pyridoxine-dependent epilepsy (PDE) [MIM:266100] |
|
rs2234622
|
Polymorphism |
- |
|
rs5054
|
Polymorphism |
- |
|
rs5056
|
Polymorphism |
- |
|
hsa00051
|
Fructose and mannose metabolism
|
|
dbSNP |
Type |
Disease name |
|
-
|
Disease |
Maturity-onset diabetes of the young 2 (MODY2) [MIM:125851] |
|
-
|
Disease |
Diabetes mellitus, permanent neonatal (PNDM) [MIM:606176] |
|
rs104893643
|
Disease |
Fructosuria (FRUCT) [MIM:229800] |
|
rs104893644
|
Disease |
Fructosuria (FRUCT) [MIM:229800] |
|
rs1375656631
|
Disease |
Maturity-onset diabetes of the young 2 (MODY2) [MIM:125851] |
|
rs1441649062
|
Disease |
Maturity-onset diabetes of the young 2 (MODY2) [MIM:125851] |
|
rs148311934
|
Disease |
Maturity-onset diabetes of the young 2 (MODY2) [MIM:125851] |
|
rs1554335135
|
Disease |
Maturity-onset diabetes of the young 2 (MODY2) [MIM:125851] |
|
rs193922297
|
Disease |
Maturity-onset diabetes of the young 2 (MODY2) [MIM:125851] |
|
rs398122379
|
Disease |
Hexokinase deficiency (HK deficiency) [MIM:235700] |
|
rs769268803
|
Disease |
Maturity-onset diabetes of the young 2 (MODY2) [MIM:125851] |
|
rs80356655
|
Disease |
Maturity-onset diabetes of the young 2 (MODY2) [MIM:125851] |
|
rs80356655
|
Disease |
Diabetes mellitus, permanent neonatal (PNDM) [MIM:606176] |
|
hsa00052
|
Galactose metabolism
|
|
dbSNP |
Type |
Disease name |
|
-
|
Disease |
Maturity-onset diabetes of the young 2 (MODY2) [MIM:125851] |
|
-
|
Disease |
Galactosemia II (GALCT2) [MIM:230200] |
|
-
|
Disease |
GM1-gangliosidosis 1 (GM1G1) [MIM:230500] |
|
-
|
Disease |
GM1-gangliosidosis 2 (GM1G2) [MIM:230600] |
|
-
|
Disease |
Glycogen storage disease 2 (GSD2) [MIM:232300] |
|
-
|
Disease |
Fabry disease (FD) [MIM:301500] |
|
-
|
Disease |
Diabetes mellitus, permanent neonatal (PNDM) [MIM:606176] |
|
-
|
Disease |
Congenital disorder of glycosylation 1T (CDG1T) [MIM:614921] |
|
rs104894009
|
Disease |
Maturity-onset diabetes of the young 2 (MODY2) [MIM:125851] |
|
rs104894835
|
Disease |
Fabry disease (FD) [MIM:301500] |
|
rs104894840
|
Disease |
Fabry disease (FD) [MIM:301500] |
|
rs104894845
|
Unclassified |
Fabry disease (FD) [MIM:301500] |
|
rs1057516600
|
Disease |
Glycogen storage disease 2 (GSD2) [MIM:232300] |
|
rs111033648
|
Disease |
Galactosemia (GALCT) [MIM:230400] |
|
rs111033652
|
Disease |
Galactosemia (GALCT) [MIM:230400] |
|
rs111033669
|
Disease |
Galactosemia (GALCT) [MIM:230400] |
|
rs111033715
|
Disease |
Galactosemia (GALCT) [MIM:230400] |
|
rs111033720
|
Disease |
Galactosemia (GALCT) [MIM:230400] |
|
rs111033802
|
Disease |
Galactosemia (GALCT) [MIM:230400] |
|
rs111033808
|
Disease |
Galactosemia (GALCT) [MIM:230400] |
|
rs111033809
|
Disease |
Galactosemia (GALCT) [MIM:230400] |
|
rs111033810
|
Disease |
Galactosemia (GALCT) [MIM:230400] |
|
rs111033812
|
Disease |
Galactosemia (GALCT) [MIM:230400] |
|
rs111033814
|
Disease |
Galactosemia (GALCT) [MIM:230400] |
|
rs111033815
|
Disease |
Galactosemia (GALCT) [MIM:230400] |
|
rs111033832
|
Disease |
Galactosemia (GALCT) [MIM:230400] |
|
rs1131691416
|
Disease |
Maturity-onset diabetes of the young 2 (MODY2) [MIM:125851] |
|
rs113173389
|
Disease |
Fabry disease (FD) [MIM:301500] |
|
rs121908047
|
Disease |
Epimerase-deficiency galactosemia (EDG) [MIM:230350] |
|
rs1286804191
|
Disease |
Diabetes mellitus, permanent neonatal (PNDM) [MIM:606176] |
|
rs1320810473
|
Disease |
Congenital disorder of glycosylation 1T (CDG1T) [MIM:614921] |
|
rs1375656631
|
Disease |
Maturity-onset diabetes of the young 2 (MODY2) [MIM:125851] |
|
rs137853860
|
Disease |
Epimerase-deficiency galactosemia (EDG) [MIM:230350] |
|
rs137853861
|
Disease |
Epimerase-deficiency galactosemia (EDG) [MIM:230350] |
|
rs141533320
|
Disease |
Glycogen storage disease 2 (GSD2) [MIM:232300] |
|
rs142752477
|
Disease |
Glycogen storage disease 2 (GSD2) [MIM:232300] |
|
rs1441649062
|
Disease |
Maturity-onset diabetes of the young 2 (MODY2) [MIM:125851] |
|
rs148311934
|
Disease |
Maturity-onset diabetes of the young 2 (MODY2) [MIM:125851] |
|
rs1553612220
|
Disease |
Mucopolysaccharidosis 4B (MPS4B) [MIM:253010] |
|
rs1554335135
|
Disease |
Maturity-onset diabetes of the young 2 (MODY2) [MIM:125851] |
|
rs1555748926
|
Disease |
Galactosemia II (GALCT2) [MIM:230200] |
|
rs1800299
|
Polymorphism |
- |
|
rs193922272
|
Disease |
Maturity-onset diabetes of the young 2 (MODY2) [MIM:125851] |
|
rs193922282
|
Disease |
Diabetes mellitus, permanent neonatal (PNDM) [MIM:606176] |
|
rs193922297
|
Disease |
Maturity-onset diabetes of the young 2 (MODY2) [MIM:125851] |
|
rs193922311
|
Disease |
Maturity-onset diabetes of the young 2 (MODY2) [MIM:125851] |
|
rs367543259
|
Disease |
Galactosemia (GALCT) [MIM:230400] |
|
rs368438393
|
Disease |
Glycogen storage disease 2 (GSD2) [MIM:232300] |
|
rs375690568
|
Disease |
Galactosemia II (GALCT2) [MIM:230200] |
|
rs376663785
|
Disease |
GM1-gangliosidosis 3 (GM1G3) [MIM:230650] |
|
rs398122379
|
Disease |
Hexokinase deficiency (HK deficiency) [MIM:235700] |
|
rs5054
|
Polymorphism |
- |
|
rs5056
|
Polymorphism |
- |
|
rs549029029
|
Disease |
Glycogen storage disease 2 (GSD2) [MIM:232300] |
|
rs72555362
|
Disease |
Mucopolysaccharidosis 4B (MPS4B) [MIM:253010] |
|
rs727505292
|
Unclassified |
Fabry disease (FD) [MIM:301500] |
|
rs730880451
|
Disease |
Fabry disease (FD) [MIM:301500] |
|
rs75391579
|
Disease |
Galactosemia (GALCT) [MIM:230400] |
|
rs754967473
|
Disease |
Galactosemia II (GALCT2) [MIM:230200] |
|
rs758737171
|
Disease |
Familial hyperinsulinemic hypoglycemia 3 (HHF3) [MIM:602485] |
|
rs764670084
|
Disease |
Glycogen storage disease 2 (GSD2) [MIM:232300] |
|
rs769268803
|
Disease |
Maturity-onset diabetes of the young 2 (MODY2) [MIM:125851] |
|
rs772883420
|
Disease |
Glycogen storage disease 2 (GSD2) [MIM:232300] |
|
rs773416476
|
Polymorphism |
- |
|
rs80356655
|
Disease |
Maturity-onset diabetes of the young 2 (MODY2) [MIM:125851] |
|
rs80356655
|
Disease |
Diabetes mellitus, permanent neonatal (PNDM) [MIM:606176] |
|
rs869312136
|
Unclassified |
Fabry disease (FD) [MIM:301500] |
|
rs869312137
|
Unclassified |
Fabry disease (FD) [MIM:301500] |
|
rs869312138
|
Disease |
Fabry disease (FD) [MIM:301500] |
|
rs869312153
|
Unclassified |
Fabry disease (FD) [MIM:301500] |
|
rs869312159
|
Unclassified |
Fabry disease (FD) [MIM:301500] |
|
rs869312160
|
Disease |
Fabry disease (FD) [MIM:301500] |
|
rs869312161
|
Unclassified |
Fabry disease (FD) [MIM:301500] |
|
rs869312163
|
Disease |
Fabry disease (FD) [MIM:301500] |
|
rs869312214
|
Disease |
Fabry disease (FD) [MIM:301500] |
|
rs869312254
|
Disease |
Fabry disease (FD) [MIM:301500] |
|
rs869312256
|
Disease |
Fabry disease (FD) [MIM:301500] |
|
rs869312270
|
Disease |
Fabry disease (FD) [MIM:301500] |
|
rs869312393
|
Disease |
Fabry disease (FD) [MIM:301500] |
|
rs869312399
|
Disease |
Fabry disease (FD) [MIM:301500] |
|
rs879050821
|
Disease |
GM1-gangliosidosis 1 (GM1G1) [MIM:230500] |
|
rs886041315
|
Disease |
Fabry disease (FD) [MIM:301500] |
|
rs886042079
|
Polymorphism |
- |
|
rs886044845
|
Disease |
Fabry disease (FD) [MIM:301500] |
|
rs968221254
|
Disease |
Mucopolysaccharidosis 4B (MPS4B) [MIM:253010] |
|
hsa00053
|
Ascorbate and aldarate metabolism
|
|
dbSNP |
Type |
Disease name |
|
rs11509436
|
Polymorphism |
- |
|
rs11509438
|
Polymorphism |
- |
|
rs11509439
|
Polymorphism |
- |
|
rs121912707
|
Disease |
Pyridoxine-dependent epilepsy (PDE) [MIM:266100] |
|
rs121912711
|
Disease |
Pyridoxine-dependent epilepsy (PDE) [MIM:266100] |
|
hsa00061
|
Fatty acid biosynthesis
|
|
dbSNP |
Type |
Disease name |
|
rs113931914
|
Polymorphism |
- |
|
rs1357271377
|
Unclassified |
A colorectal cancer sample |
|
rs2228307
|
Polymorphism |
- |
|
hsa00062
|
Fatty acid elongation
|
|
dbSNP |
Type |
Disease name |
|
rs104886492
|
Unclassified |
HDS10 mitochondrial disease (HSD10MD) [MIM:300438] |
|
rs11544658
|
Polymorphism |
- |
|
rs120074140
|
Disease |
3-ketothiolase deficiency (3KTD) [MIM:203750] |
|
rs120074141
|
Disease |
3-ketothiolase deficiency (3KTD) [MIM:203750] |
|
rs120074145
|
Disease |
3-ketothiolase deficiency (3KTD) [MIM:203750] |
|
rs137853096
|
Disease |
D-bifunctional protein deficiency (DBPD) [MIM:261515] |
|
rs137853101
|
Disease |
3-alpha-hydroxyacyl-CoA dehydrogenase deficiency (HADH deficiency) [MIM:231530] |
|
rs137853102
|
Disease |
3-alpha-hydroxyacyl-CoA dehydrogenase deficiency (HADH deficiency) [MIM:231530] |
|
rs759218713
|
Disease |
Dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities (DYTOABG) [MIM:617282] |
|
hsa00071
|
Fatty acid degradation
|
|
dbSNP |
Type |
Disease name |
|
-
|
Disease |
Microphthalmia, isolated, 8 (MCOP8) [MIM:615113] |
|
rs1041969
|
Polymorphism |
- |
|
rs104886492
|
Unclassified |
HDS10 mitochondrial disease (HSD10MD) [MIM:300438] |
|
rs120074140
|
Disease |
3-ketothiolase deficiency (3KTD) [MIM:203750] |
|
rs120074141
|
Disease |
3-ketothiolase deficiency (3KTD) [MIM:203750] |
|
rs120074145
|
Disease |
3-ketothiolase deficiency (3KTD) [MIM:203750] |
|
rs121434275
|
Disease |
Acyl-CoA dehydrogenase medium-chain deficiency (ACADMD) [MIM:201450] |
|
rs121434278
|
Disease |
Acyl-CoA dehydrogenase medium-chain deficiency (ACADMD) [MIM:201450] |
|
rs121434279
|
Disease |
Acyl-CoA dehydrogenase medium-chain deficiency (ACADMD) [MIM:201450] |
|
rs121434281
|
Disease |
Acyl-CoA dehydrogenase medium-chain deficiency (ACADMD) [MIM:201450] |
|
rs121434283
|
Disease |
Acyl-CoA dehydrogenase medium-chain deficiency (ACADMD) [MIM:201450] |
|
rs121912707
|
Disease |
Pyridoxine-dependent epilepsy (PDE) [MIM:266100] |
|
rs121912711
|
Disease |
Pyridoxine-dependent epilepsy (PDE) [MIM:266100] |
|
rs1229984
|
Polymorphism |
- |
|
rs137853096
|
Disease |
D-bifunctional protein deficiency (DBPD) [MIM:261515] |
|
rs137853101
|
Disease |
3-alpha-hydroxyacyl-CoA dehydrogenase deficiency (HADH deficiency) [MIM:231530] |
|
rs137853102
|
Disease |
3-alpha-hydroxyacyl-CoA dehydrogenase deficiency (HADH deficiency) [MIM:231530] |
|
rs2066702
|
Polymorphism |
- |
|
rs28730628
|
Polymorphism |
- |
|
rs35385902
|
Polymorphism |
- |
|
hsa00072
|
Synthesis and degradation of ketone bodies
|
|
dbSNP |
Type |
Disease name |
|
-
|
Disease |
Succinyl-CoA:3-oxoacid CoA transferase deficiency (SCOTD) [MIM:245050] |
|
-
|
Disease |
3-hydroxy-3-methylglutaryl-CoA lyase deficiency (HMGCLD) [MIM:246450] |
|
rs120074141
|
Disease |
3-ketothiolase deficiency (3KTD) [MIM:203750] |
|
rs121909301
|
Disease |
Succinyl-CoA:3-oxoacid CoA transferase deficiency (SCOTD) [MIM:245050] |
|
rs1327401976
|
Disease |
Succinyl-CoA:3-oxoacid CoA transferase deficiency (SCOTD) [MIM:245050] |
|
rs1357942068
|
Disease |
3-hydroxy-3-methylglutaryl-CoA lyase deficiency (HMGCLD) [MIM:246450] |
|
rs137852640
|
Disease |
3-hydroxy-3-methylglutaryl-CoA synthase-2 deficiency (HMGCS2D) [MIM:605911] |
|
rs1553131940
|
Disease |
3-hydroxy-3-methylglutaryl-CoA lyase deficiency (HMGCLD) [MIM:246450] |
|
rs199587895
|
Disease |
3-hydroxy-3-methylglutaryl-CoA lyase deficiency (HMGCLD) [MIM:246450] |
|
rs727503963
|
Disease |
3-hydroxy-3-methylglutaryl-CoA lyase deficiency (HMGCLD) [MIM:246450] |
|
rs760106433
|
Disease |
3-hydroxy-3-methylglutaryl-CoA lyase deficiency (HMGCLD) [MIM:246450] |
|
hsa00100
|
Steroid biosynthesis
|
|
dbSNP |
Type |
Disease name |
|
-
|
Unclassified |
Hypotrichosis 14 (HYPT14) [MIM:618275] |
|
rs4731
|
Polymorphism |
- |
|
rs864622780
|
Disease |
Cataract 44 (CTRCT44) [MIM:616509] |
|
hsa00120
|
Primary bile acid biosynthesis
|
|
dbSNP |
Type |
Disease name |
|
rs104886492
|
Unclassified |
HDS10 mitochondrial disease (HSD10MD) [MIM:300438] |
|
rs1057909
|
Polymorphism |
- |
|
rs1228918719
|
Disease |
Congenital bile acid synthesis defect 2 (CBAS2) [MIM:235555] |
|
rs137853096
|
Disease |
D-bifunctional protein deficiency (DBPD) [MIM:261515] |
|
rs137853101
|
Disease |
3-alpha-hydroxyacyl-CoA dehydrogenase deficiency (HADH deficiency) [MIM:231530] |
|
rs137853102
|
Disease |
3-alpha-hydroxyacyl-CoA dehydrogenase deficiency (HADH deficiency) [MIM:231530] |
|
rs1799853
|
Polymorphism |
- |
|
rs28371686
|
Polymorphism |
- |
|
rs56165452
|
Polymorphism |
- |
|
hsa00130
|
Ubiquinone and other terpenoid-quinone biosynthesis
|
|
dbSNP |
Type |
Disease name |
|
-
|
Disease |
Tyrosinemia 3 (TYRSN3) [MIM:276710] |
|
rs137852865
|
Disease |
Tyrosinemia 3 (TYRSN3) [MIM:276710] |
|
hsa00140
|
Steroid hormone biosynthesis
|
|
dbSNP |
Type |
Disease name |
|
-
|
Disease |
Adrenal hyperplasia 5 (AH5) [MIM:202110] |
|
-
|
Disease |
Glaucoma 3, primary congenital, A (GLC3A) [MIM:231300] |
|
-
|
Disease |
46,XY sex reversal 8 (SRXY8) [MIM:614279] |
|
rs104893628
|
Disease |
Glaucoma 3, primary congenital, A (GLC3A) [MIM:231300] |
|
rs104894135
|
Disease |
Adrenal hyperplasia 5 (AH5) [MIM:202110] |
|
rs104894139
|
Disease |
Adrenal hyperplasia 5 (AH5) [MIM:202110] |
|
rs104894140
|
Disease |
Adrenal hyperplasia 5 (AH5) [MIM:202110] |
|
rs104894142
|
Disease |
Adrenal hyperplasia 5 (AH5) [MIM:202110] |
|
rs104894146
|
Disease |
Adrenal hyperplasia 5 (AH5) [MIM:202110] |
|
rs104894147
|
Disease |
Adrenal hyperplasia 5 (AH5) [MIM:202110] |
|
rs104894149
|
Disease |
Adrenal hyperplasia 5 (AH5) [MIM:202110] |
|
rs104894153
|
Disease |
Adrenal hyperplasia 5 (AH5) [MIM:202110] |
|
rs11569705
|
Polymorphism |
- |
|
rs121434534
|
Disease |
Aromatase deficiency (AROD) [MIM:613546] |
|
rs121912978
|
Disease |
Corticosterone methyloxidase 2 deficiency (CMO-2 deficiency) [MIM:610600] |
|
rs1228918719
|
Disease |
Congenital bile acid synthesis defect 2 (CBAS2) [MIM:235555] |
|
rs12721627
|
Polymorphism |
- |
|
rs12721629
|
Polymorphism |
- |
|
rs137853166
|
Disease |
Ichthyosis, X-linked (IXL) [MIM:308100] |
|
rs137853168
|
Disease |
Ichthyosis, X-linked (IXL) [MIM:308100] |
|
rs1423560123
|
Disease |
Adrenal hyperplasia 5 (AH5) [MIM:202110] |
|
rs147402365
|
Polymorphism |
- |
|
rs148542782
|
Disease |
Glaucoma 3, primary congenital, A (GLC3A) [MIM:231300] |
|
rs28371759
|
Polymorphism |
- |
|
rs2854482
|
Polymorphism |
- |
|
rs28936701
|
Disease |
Glaucoma 3, primary congenital, A (GLC3A) [MIM:231300] |
|
rs3208363
|
Polymorphism |
- |
|
rs4539
|
Polymorphism |
- |
|
rs4986871
|
Polymorphism |
- |
|
rs4986910
|
Polymorphism |
- |
|
rs4987161
|
Polymorphism |
- |
|
rs5312
|
Polymorphism |
- |
|
rs5317
|
Polymorphism |
- |
|
rs55785340
|
Polymorphism |
- |
|
rs55901263
|
Polymorphism |
- |
|
rs55951658
|
Polymorphism |
- |
|
rs55989760
|
Disease |
Glaucoma 3, primary congenital, A (GLC3A) [MIM:231300] |
|
rs56324128
|
Polymorphism |
- |
|
rs57865060
|
Disease |
Glaucoma 3, primary congenital, A (GLC3A) [MIM:231300] |
|
rs66583685
|
Disease |
Glaucoma 3, primary congenital, A (GLC3A) [MIM:231300] |
|
rs67784355
|
Polymorphism |
- |
|
rs72549378
|
Disease |
Glaucoma 3, primary congenital, A (GLC3A) [MIM:231300] |
|
rs72552799
|
Polymorphism |
- |
|
rs752456881
|
Polymorphism |
- |
|
rs762631156
|
Polymorphism |
- |
|
rs777638364
|
Disease |
Adrenal hyperplasia 5 (AH5) [MIM:202110] |
|
rs78310315
|
Disease |
Aromatase deficiency (AROD) [MIM:613546] |
|
rs9282670
|
Polymorphism |
- |
|
rs9341250
|
Polymorphism |
- |
|
hsa00220
|
Arginine biosynthesis
|
|
dbSNP |
Type |
Disease name |
|
-
|
Disease |
Argininemia (ARGIN) [MIM:207800] |
|
-
|
Disease |
Citrullinemia 1 (CTLN1) [MIM:215700] |
|
-
|
Disease |
Carbamoyl phosphate synthetase 1 deficiency (CPS1D) [MIM:237300] |
|
-
|
Disease |
Infantile cataract, skin abnormalities, glutamate excess, and impaired intellectual development (CASGID) [MIM:618339] |
|
rs1048119191
|
Disease |
Carbamoyl phosphate synthetase 1 deficiency (CPS1D) [MIM:237300] |
|
rs104893943
|
Disease |
Argininemia (ARGIN) [MIM:207800] |
|
rs115014558
|
Polymorphism |
- |
|
rs1202306773
|
Disease |
Carbamoyl phosphate synthetase 1 deficiency (CPS1D) [MIM:237300] |
|
rs121908638
|
Disease |
Citrullinemia 1 (CTLN1) [MIM:215700] |
|
rs121912592
|
Disease |
Carbamoyl phosphate synthetase 1 deficiency (CPS1D) [MIM:237300] |
|
rs1275599086
|
Disease |
Carbamoyl phosphate synthetase 1 deficiency (CPS1D) [MIM:237300] |
|
rs1280211937
|
Disease |
Carbamoyl phosphate synthetase 1 deficiency (CPS1D) [MIM:237300] |
|
rs1319489001
|
Disease |
Carbamoyl phosphate synthetase 1 deficiency (CPS1D) [MIM:237300] |
|
rs13408961
|
Polymorphism |
- |
|
rs1392934477
|
Disease |
Carbamoyl phosphate synthetase 1 deficiency (CPS1D) [MIM:237300] |
|
rs140992177
|
Polymorphism |
- |
|
rs1553513429
|
Disease |
Carbamoyl phosphate synthetase 1 deficiency (CPS1D) [MIM:237300] |
|
rs1553516442
|
Disease |
Carbamoyl phosphate synthetase 1 deficiency (CPS1D) [MIM:237300] |
|
rs180177155
|
Disease |
Hyperoxaluria primary 1 (HP1) [MIM:259900] |
|
rs180177156
|
Disease |
Hyperoxaluria primary 1 (HP1) [MIM:259900] |
|
rs180177157
|
Disease |
Hyperoxaluria primary 1 (HP1) [MIM:259900] |
|
rs180177173
|
Disease |
Hyperoxaluria primary 1 (HP1) [MIM:259900] |
|
rs180177197
|
Disease |
Hyperoxaluria primary 1 (HP1) [MIM:259900] |
|
rs180177225
|
Disease |
Hyperoxaluria primary 1 (HP1) [MIM:259900] |
|
rs180177244
|
Disease |
Hyperoxaluria primary 1 (HP1) [MIM:259900] |
|
rs180177264
|
Disease |
Hyperoxaluria primary 1 (HP1) [MIM:259900] |
|
rs180177290
|
Disease |
Hyperoxaluria primary 1 (HP1) [MIM:259900] |
|
rs201623252
|
Polymorphism |
- |
|
rs34885252
|
Polymorphism |
- |
|
rs369061090
|
Disease |
Carbamoyl phosphate synthetase 1 deficiency (CPS1D) [MIM:237300] |
|
rs371265106
|
Disease |
Citrullinemia 1 (CTLN1) [MIM:215700] |
|
rs4426527
|
Polymorphism |
- |
|
rs66550389
|
Disease |
Ornithine carbamoyltransferase deficiency (OTCD) [MIM:311250] |
|
rs66626662
|
Disease |
Ornithine carbamoyltransferase deficiency (OTCD) [MIM:311250] |
|
rs66642398
|
Disease |
Ornithine carbamoyltransferase deficiency (OTCD) [MIM:311250] |
|
rs66867430
|
Disease |
Ornithine carbamoyltransferase deficiency (OTCD) [MIM:311250] |
|
rs67156896
|
Disease |
Ornithine carbamoyltransferase deficiency (OTCD) [MIM:311250] |
|
rs67501347
|
Disease |
Ornithine carbamoyltransferase deficiency (OTCD) [MIM:311250] |
|
rs68026851
|
Disease |
Ornithine carbamoyltransferase deficiency (OTCD) [MIM:311250] |
|
rs72554331
|
Disease |
Ornithine carbamoyltransferase deficiency (OTCD) [MIM:311250] |
|
rs72554339
|
Disease |
Ornithine carbamoyltransferase deficiency (OTCD) [MIM:311250] |
|
rs72554342
|
Disease |
Ornithine carbamoyltransferase deficiency (OTCD) [MIM:311250] |
|
rs72554344
|
Disease |
Ornithine carbamoyltransferase deficiency (OTCD) [MIM:311250] |
|
rs72558404
|
Disease |
Ornithine carbamoyltransferase deficiency (OTCD) [MIM:311250] |
|
rs72558407
|
Disease |
Ornithine carbamoyltransferase deficiency (OTCD) [MIM:311250] |
|
rs72558442
|
Disease |
Ornithine carbamoyltransferase deficiency (OTCD) [MIM:311250] |
|
rs72558448
|
Disease |
Ornithine carbamoyltransferase deficiency (OTCD) [MIM:311250] |
|
rs72558449
|
Disease |
Ornithine carbamoyltransferase deficiency (OTCD) [MIM:311250] |
|
rs72558450
|
Disease |
Ornithine carbamoyltransferase deficiency (OTCD) [MIM:311250] |
|
rs72558463
|
Disease |
Ornithine carbamoyltransferase deficiency (OTCD) [MIM:311250] |
|
rs72558464
|
Disease |
Ornithine carbamoyltransferase deficiency (OTCD) [MIM:311250] |
|
rs72558465
|
Disease |
Ornithine carbamoyltransferase deficiency (OTCD) [MIM:311250] |
|
rs72558478
|
Disease |
Ornithine carbamoyltransferase deficiency (OTCD) [MIM:311250] |
|
rs73106685
|
Polymorphism |
- |
|
rs750670270
|
Disease |
Carbamoyl phosphate synthetase 1 deficiency (CPS1D) [MIM:237300] |
|
rs752339705
|
Disease |
Carbamoyl phosphate synthetase 1 deficiency (CPS1D) [MIM:237300] |
|
rs757205958
|
Disease |
Carbamoyl phosphate synthetase 1 deficiency (CPS1D) [MIM:237300] |
|
rs768215008
|
Disease |
Citrullinemia 1 (CTLN1) [MIM:215700] |
|
rs769018733
|
Disease |
Citrullinemia 1 (CTLN1) [MIM:215700] |
|
rs775163147
|
Disease |
Citrullinemia 1 (CTLN1) [MIM:215700] |
|
rs775305020
|
Disease |
Citrullinemia 1 (CTLN1) [MIM:215700] |
|
rs777233486
|
Disease |
Carbamoyl phosphate synthetase 1 deficiency (CPS1D) [MIM:237300] |
|
rs796052061
|
Disease |
Hyperoxaluria primary 1 (HP1) [MIM:259900] |
|
rs80358214
|
Disease |
Congenital systemic glutamine deficiency (CSGD) [MIM:610015] |
|
rs933813349
|
Disease |
Carbamoyl phosphate synthetase 1 deficiency (CPS1D) [MIM:237300] |
|
rs936192871
|
Disease |
Citrullinemia 1 (CTLN1) [MIM:215700] |
|
hsa00230
|
Purine metabolism
|
|
dbSNP |
Type |
Disease name |
|
-
|
Disease |
Microcephaly with or without chorioretinopathy, lymphedema, or mental retardation (MCLMR) [MIM:152950] |
|
-
|
Disease |
Pyruvate kinase deficiency of red cells (PKRD) [MIM:266200] |
|
-
|
Disease |
Lesch-Nyhan syndrome (LNS) [MIM:300322] |
|
-
|
Disease |
Gout HPRT-related (GOUT-HPRT) [MIM:300323] |
|
-
|
Disease |
Mental retardation, X-linked 102 (MRX102) [MIM:300958] |
|
-
|
Disease |
Neuronopathy, distal hereditary motor, 6 (HMN6) [MIM:604320] |
|
-
|
Disease |
Noonan syndrome 3 (NS3) [MIM:609942] |
|
-
|
Disease |
Retinitis pigmentosa 33 (RP33) [MIM:610359] |
|
-
|
Unclassified |
Spastic paraplegia 45, autosomal recessive (SPG45) [MIM:613162] |
|
-
|
Disease |
Adenine phosphoribosyltransferase deficiency (APRTD) [MIM:614723] |
|
rs104893631
|
Disease |
Mitochondrial DNA depletion syndrome 3 (MTDPS3) [MIM:251880] |
|
rs104893632
|
Disease |
Mitochondrial DNA depletion syndrome 3 (MTDPS3) [MIM:251880] |
|
rs104894227
|
Disease |
Costello syndrome (CSTLO) [MIM:218040] |
|
rs104894228
|
Disease |
Schimmelpenning-Feuerstein-Mims syndrome (SFM) [MIM:163200] |
|
rs104894230
|
Disease |
Costello syndrome (CSTLO) [MIM:218040] |
|
rs104894359
|
Disease |
Noonan syndrome 3 (NS3) [MIM:609942] |
|
rs104894364
|
Disease |
Noonan syndrome 3 (NS3) [MIM:609942] |
|
rs104894365
|
Disease |
Noonan syndrome 3 (NS3) [MIM:609942] |
|
rs104894451
|
Disease |
Purine nucleoside phosphorylase deficiency (PNPD) [MIM:613179] |
|
rs104894452
|
Disease |
Purine nucleoside phosphorylase deficiency (PNPD) [MIM:613179] |
|
rs104894506
|
Disease |
Adenine phosphoribosyltransferase deficiency (APRTD) [MIM:614723] |
|
rs104894508
|
Disease |
Adenine phosphoribosyltransferase deficiency (APRTD) [MIM:614723] |
|
rs1057519430
|
Disease |
Mental retardation, X-linked 102 (MRX102) [MIM:300958] |
|
rs1064794574
|
Disease |
Mental retardation, X-linked 102 (MRX102) [MIM:300958] |
|
rs11549976
|
Polymorphism |
- |
|
rs1167329263
|
Disease |
Pyruvate kinase deficiency of red cells (PKRD) [MIM:266200] |
|
rs1177201180
|
Disease |
Cystic fibrosis (CF) [MIM:219700] |
|
rs121908714
|
Disease |
Severe combined immunodeficiency autosomal recessive T-cell-negative/B-cell-negative/NK-cell-negative due to adenosine deaminase deficiency (ADASCID) [MIM:102700] |
|
rs121908724
|
Disease |
Severe combined immunodeficiency autosomal recessive T-cell-negative/B-cell-negative/NK-cell-negative due to adenosine deaminase deficiency (ADASCID) [MIM:102700] |
|
rs121908725
|
Disease |
Severe combined immunodeficiency autosomal recessive T-cell-negative/B-cell-negative/NK-cell-negative due to adenosine deaminase deficiency (ADASCID) [MIM:102700] |
|
rs121908759
|
Unclassified |
Congenital bilateral absence of the vas deferens (CBAVD) [MIM:277180] |
|
rs121908951
|
Disease |
Brachyolmia type 4 with mild epiphyseal and metaphyseal changes (BCYM4) [MIM:612847] |
|
rs121909009
|
Disease |
Cystic fibrosis (CF) [MIM:219700] |
|
rs121909033
|
Disease |
Cystic fibrosis (CF) [MIM:219700] |
|
rs121913240
|
Unclassified |
A colorectal cancer sample |
|
rs121913527
|
Unclassified |
A colorectal cancer sample |
|
rs121913528
|
Disease |
Gastric cancer (GASC) [MIM:613659] |
|
rs121913529
|
Unclassified |
A colorectal cancer sample |
|
rs121913535
|
Polymorphism |
- |
|
rs121917758
|
Disease |
Costello syndrome (CSTLO) [MIM:218040] |
|
rs121917759
|
Disease |
Costello syndrome (CSTLO) [MIM:218040] |
|
rs121917887
|
Polymorphism |
- |
|
rs137852485
|
Disease |
Gout HPRT-related (GOUT-HPRT) [MIM:300323] |
|
rs137852487
|
Disease |
Lesch-Nyhan syndrome (LNS) [MIM:300322] |
|
rs137852488
|
Disease |
Lesch-Nyhan syndrome (LNS) [MIM:300322] |
|
rs137852496
|
Disease |
Lesch-Nyhan syndrome (LNS) [MIM:300322] |
|
rs137852498
|
Disease |
Gout HPRT-related (GOUT-HPRT) [MIM:300323] |
|
rs137852543
|
Disease |
Phosphoribosylpyrophosphate synthetase superactivity (PRPS1 superactivity) [MIM:300661] |
|
rs137852545
|
Disease |
Phosphoribosylpyrophosphate synthetase superactivity (PRPS1 superactivity) [MIM:300661] |
|
rs144181978
|
Disease |
Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 4 (PEOB4) [MIM:617070] |
|
rs1465803265
|
Disease |
Neuronopathy, distal hereditary motor, 6 (HMN6) [MIM:604320] |
|
rs150181226
|
Disease |
Desbuquois dysplasia 1 (DBQD1) [MIM:251450] |
|
rs1554263326
|
Disease |
Mental retardation, autosomal dominant 48 (MRD48) [MIM:617751] |
|
rs1554264268
|
Disease |
Mental retardation, autosomal dominant 48 (MRD48) [MIM:617751] |
|
rs1555690779
|
Disease |
Neurodevelopmental disorder with ataxic gait, absent speech, and decreased cortical white matter (NDAGSCW) [MIM:617807] |
|
rs1555690804
|
Disease |
Neurodevelopmental disorder with ataxic gait, absent speech, and decreased cortical white matter (NDAGSCW) [MIM:617807] |
|
rs17853396
|
Polymorphism |
- |
|
rs1800089
|
Polymorphism |
- |
|
rs267606635
|
Unclassified |
Severe combined immunodeficiency autosomal recessive T-cell-negative/B-cell-negative/NK-cell-negative due to adenosine deaminase deficiency (ADASCID) [MIM:102700] |
|
rs267606699
|
Disease |
Desbuquois dysplasia 1 (DBQD1) [MIM:251450] |
|
rs267606700
|
Disease |
Desbuquois dysplasia 1 (DBQD1) [MIM:251450] |
|
rs267606863
|
Disease |
Lesch-Nyhan syndrome (LNS) [MIM:300322] |
|
rs28933406
|
Disease |
Thyroid cancer, non-medullary, 2 (NMTC2) [MIM:188470] |
|
rs28999113
|
Disease |
Adenine phosphoribosyltransferase deficiency (APRTD) [MIM:614723] |
|
rs34082669
|
Polymorphism |
- |
|
rs34354104
|
Polymorphism |
- |
|
rs35698797
|
Polymorphism |
- |
|
rs373458753
|
Disease |
Adenylosuccinase deficiency (ADSLD) [MIM:103050] |
|
rs374259530
|
Disease |
Adenylosuccinase deficiency (ADSLD) [MIM:103050] |
|
rs387906643
|
Disease |
Microcephaly with or without chorioretinopathy, lymphedema, or mental retardation (MCLMR) [MIM:152950] |
|
rs387907206
|
Disease |
Cardiofaciocutaneous syndrome 2 (CFC2) [MIM:615278] |
|
rs397508195
|
Disease |
Cystic fibrosis (CF) [MIM:219700] |
|
rs397508282
|
Disease |
Cystic fibrosis (CF) [MIM:219700] |
|
rs397508288
|
Disease |
Cystic fibrosis (CF) [MIM:219700] |
|
rs397508313
|
Disease |
Cystic fibrosis (CF) [MIM:219700] |
|
rs397514452
|
Disease |
Hypermethioninemia due to adenosine kinase deficiency (HMAKD) [MIM:614300] |
|
rs397514454
|
Disease |
Hypermethioninemia due to adenosine kinase deficiency (HMAKD) [MIM:614300] |
|
rs397514469
|
Disease |
Acrodysostosis 2, with or without hormone resistance (ACRDYS2) [MIM:614613] |
|
rs5832
|
Polymorphism |
- |
|
rs5837
|
Polymorphism |
- |
|
rs587777188
|
Disease |
Acrodysostosis 2, with or without hormone resistance (ACRDYS2) [MIM:614613] |
|
rs587777861
|
Disease |
Epileptic encephalopathy, early infantile, 31 (EIEE31) [MIM:616346] |
|
rs72554654
|
Disease |
Menkes disease (MNKD) [MIM:309400] |
|
rs727503109
|
Disease |
Noonan syndrome 3 (NS3) [MIM:609942] |
|
rs727503110
|
Disease |
Noonan syndrome 3 (NS3) [MIM:609942] |
|
rs746930990
|
Unclassified |
Epileptic encephalopathy, early infantile, 35 (EIEE35) [MIM:616647] |
|
rs747097960
|
Disease |
Pyruvate kinase deficiency of red cells (PKRD) [MIM:266200] |
|
rs747281324
|
Disease |
Bloom syndrome (BLM) [MIM:210900] |
|
rs749246739
|
Disease |
Desbuquois dysplasia 1 (DBQD1) [MIM:251450] |
|
rs760270633
|
Disease |
Epileptic encephalopathy, early infantile, 31 (EIEE31) [MIM:616346] |
|
rs762550967
|
Disease |
Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 4 (PEOB4) [MIM:617070] |
|
rs763615602
|
Disease |
Portal hypertension, non-cirrhotic (NCPH) [MIM:617068] |
|
rs770248150
|
Unclassified |
A colorectal cancer sample |
|
rs780526529
|
Disease |
Cystic fibrosis (CF) [MIM:219700] |
|
rs786204847
|
Disease |
Singleton-Merten syndrome 2 (SGMRT2) [MIM:616298] |
|
rs786204848
|
Disease |
Singleton-Merten syndrome 2 (SGMRT2) [MIM:616298] |
|
rs796052223
|
Disease |
Mental retardation, X-linked 102 (MRX102) [MIM:300958] |
|
rs796052231
|
Disease |
Mental retardation, X-linked 102 (MRX102) [MIM:300958] |
|
rs797045025
|
Disease |
Mental retardation, X-linked 102 (MRX102) [MIM:300958] |
|
rs80338675
|
Disease |
ARTS syndrome (ARTS) [MIM:301835] |
|
rs875989840
|
Disease |
Striatal degeneration, autosomal dominant 2 (ADSD2) [MIM:616922] |
|
rs875989841
|
Disease |
Striatal degeneration, autosomal dominant 2 (ADSD2) [MIM:616922] |
|
rs879255688
|
Disease |
Encephalopathy due to defective mitochondrial and peroxisomal fission 1 (EMPF1) [MIM:614388] |
|
rs981505482
|
Disease |
Pyruvate kinase deficiency of red cells (PKRD) [MIM:266200] |
|
hsa00232
|
Caffeine metabolism
|
|
dbSNP |
Type |
Disease name |
|
-
|
Disease |
Glaucoma 3, primary congenital, A (GLC3A) [MIM:231300] |
|
rs104893628
|
Disease |
Glaucoma 3, primary congenital, A (GLC3A) [MIM:231300] |
|
rs148542782
|
Disease |
Glaucoma 3, primary congenital, A (GLC3A) [MIM:231300] |
|
rs28936701
|
Disease |
Glaucoma 3, primary congenital, A (GLC3A) [MIM:231300] |
|
rs55989760
|
Disease |
Glaucoma 3, primary congenital, A (GLC3A) [MIM:231300] |
|
rs57865060
|
Disease |
Glaucoma 3, primary congenital, A (GLC3A) [MIM:231300] |
|
rs66583685
|
Disease |
Glaucoma 3, primary congenital, A (GLC3A) [MIM:231300] |
|
rs669884
|
Polymorphism |
- |
|
rs72549378
|
Disease |
Glaucoma 3, primary congenital, A (GLC3A) [MIM:231300] |
|
rs752456881
|
Polymorphism |
- |
|
rs9341250
|
Polymorphism |
- |
|
hsa00240
|
Pyrimidine metabolism
|
|
dbSNP |
Type |
Disease name |
|
-
|
Disease |
Desbuquois dysplasia 1 (DBQD1) [MIM:251450] |
|
-
|
Disease |
Postaxial acrofacial dysostosis (POADS) [MIM:263750] |
|
-
|
Unclassified |
Spastic paraplegia 45, autosomal recessive (SPG45) [MIM:613162] |
|
rs104894452
|
Disease |
Purine nucleoside phosphorylase deficiency (PNPD) [MIM:613179] |
|
rs121913037
|
Disease |
Mitochondrial DNA depletion syndrome 1, MNGIE type (MTDPS1) [MIM:603041] |
|
rs121917887
|
Polymorphism |
- |
|
rs1270571213
|
Disease |
Interstitial nephritis, karyomegalic (KMIN) [MIM:614817] |
|
rs149977726
|
Disease |
Mitochondrial DNA depletion syndrome 1, MNGIE type (MTDPS1) [MIM:603041] |
|
rs150181226
|
Disease |
Desbuquois dysplasia 1 (DBQD1) [MIM:251450] |
|
rs17843776
|
Polymorphism |
- |
|
rs267606699
|
Disease |
Desbuquois dysplasia 1 (DBQD1) [MIM:251450] |
|
rs267606700
|
Disease |
Desbuquois dysplasia 1 (DBQD1) [MIM:251450] |
|
rs34082669
|
Polymorphism |
- |
|
rs749246739
|
Disease |
Desbuquois dysplasia 1 (DBQD1) [MIM:251450] |
|
rs751703979
|
Disease |
Interstitial nephritis, karyomegalic (KMIN) [MIM:614817] |
|
hsa00250
|
Alanine, aspartate and glutamate metabolism
|
|
dbSNP |
Type |
Disease name |
|
-
|
Disease |
Citrullinemia 1 (CTLN1) [MIM:215700] |
|
-
|
Disease |
Carbamoyl phosphate synthetase 1 deficiency (CPS1D) [MIM:237300] |
|
-
|
Disease |
Canavan disease (CAND) [MIM:271900] |
|
-
|
Disease |
Succinic semialdehyde dehydrogenase deficiency (SSADHD) [MIM:271980] |
|
-
|
Disease |
Infantile cataract, skin abnormalities, glutamate excess, and impaired intellectual development (CASGID) [MIM:618339] |
|
rs1014551540
|
Disease |
Canavan disease (CAND) [MIM:271900] |
|
rs1048119191
|
Disease |
Carbamoyl phosphate synthetase 1 deficiency (CPS1D) [MIM:237300] |
|
rs104894550
|
Disease |
Canavan disease (CAND) [MIM:271900] |
|
rs1057521115
|
Disease |
Canavan disease (CAND) [MIM:271900] |
|
rs115014558
|
Polymorphism |
- |
|
rs1202306773
|
Disease |
Carbamoyl phosphate synthetase 1 deficiency (CPS1D) [MIM:237300] |
|
rs121908520
|
Disease |
Hyperoxaluria primary 1 (HP1) [MIM:259900] |
|
rs121908524
|
Disease |
Hyperoxaluria primary 1 (HP1) [MIM:259900] |
|
rs121908527
|
Disease |
Hyperoxaluria primary 1 (HP1) [MIM:259900] |
|
rs121908530
|
Disease |
Hyperoxaluria primary 1 (HP1) [MIM:259900] |
|
rs121908638
|
Disease |
Citrullinemia 1 (CTLN1) [MIM:215700] |
|
rs121912592
|
Disease |
Carbamoyl phosphate synthetase 1 deficiency (CPS1D) [MIM:237300] |
|
rs1275599086
|
Disease |
Carbamoyl phosphate synthetase 1 deficiency (CPS1D) [MIM:237300] |
|
rs1280211937
|
Disease |
Carbamoyl phosphate synthetase 1 deficiency (CPS1D) [MIM:237300] |
|
rs1319489001
|
Disease |
Carbamoyl phosphate synthetase 1 deficiency (CPS1D) [MIM:237300] |
|
rs1326526453
|
Disease |
Succinic semialdehyde dehydrogenase deficiency (SSADHD) [MIM:271980] |
|
rs13408961
|
Polymorphism |
- |
|
rs137852937
|
Disease |
Hyperprolinemia 2 (HYRPRO2) [MIM:239510] |
|
rs1392934477
|
Disease |
Carbamoyl phosphate synthetase 1 deficiency (CPS1D) [MIM:237300] |
|
rs140992177
|
Polymorphism |
- |
|
rs1414684396
|
Disease |
Canavan disease (CAND) [MIM:271900] |
|
rs145087265
|
Disease |
Succinic semialdehyde dehydrogenase deficiency (SSADHD) [MIM:271980] |
|
rs1553513429
|
Disease |
Carbamoyl phosphate synthetase 1 deficiency (CPS1D) [MIM:237300] |
|
rs1553516442
|
Disease |
Carbamoyl phosphate synthetase 1 deficiency (CPS1D) [MIM:237300] |
|
rs1555538148
|
Disease |
Canavan disease (CAND) [MIM:271900] |
|
rs1555538151
|
Disease |
Canavan disease (CAND) [MIM:271900] |
|
rs180177155
|
Disease |
Hyperoxaluria primary 1 (HP1) [MIM:259900] |
|
rs180177156
|
Disease |
Hyperoxaluria primary 1 (HP1) [MIM:259900] |
|
rs180177157
|
Disease |
Hyperoxaluria primary 1 (HP1) [MIM:259900] |
|
rs180177173
|
Disease |
Hyperoxaluria primary 1 (HP1) [MIM:259900] |
|
rs180177185
|
Disease |
Hyperoxaluria primary 1 (HP1) [MIM:259900] |
|
rs180177197
|
Disease |
Hyperoxaluria primary 1 (HP1) [MIM:259900] |
|
rs180177225
|
Disease |
Hyperoxaluria primary 1 (HP1) [MIM:259900] |
|
rs180177236
|
Disease |
Hyperoxaluria primary 1 (HP1) [MIM:259900] |
|
rs180177244
|
Disease |
Hyperoxaluria primary 1 (HP1) [MIM:259900] |
|
rs180177253
|
Disease |
Hyperoxaluria primary 1 (HP1) [MIM:259900] |
|
rs180177264
|
Disease |
Hyperoxaluria primary 1 (HP1) [MIM:259900] |
|
rs180177289
|
Disease |
Hyperoxaluria primary 1 (HP1) [MIM:259900] |
|
rs180177290
|
Disease |
Hyperoxaluria primary 1 (HP1) [MIM:259900] |
|
rs201623252
|
Polymorphism |
- |
|
rs28940279
|
Disease |
Canavan disease (CAND) [MIM:271900] |
|
rs34885252
|
Polymorphism |
- |
|
rs369061090
|
Disease |
Carbamoyl phosphate synthetase 1 deficiency (CPS1D) [MIM:237300] |
|
rs371265106
|
Disease |
Citrullinemia 1 (CTLN1) [MIM:215700] |
|
rs373458753
|
Disease |
Adenylosuccinase deficiency (ADSLD) [MIM:103050] |
|
rs375628463
|
Disease |
Succinic semialdehyde dehydrogenase deficiency (SSADHD) [MIM:271980] |
|
rs398122973
|
Disease |
Asparagine synthetase deficiency (ASNSD) [MIM:615574] |
|
rs4426527
|
Polymorphism |
- |
|
rs62621664
|
Polymorphism |
- |
|
rs72552283
|
Disease |
Succinic semialdehyde dehydrogenase deficiency (SSADHD) [MIM:271980] |
|
rs73106685
|
Polymorphism |
- |
|
rs750505963
|
Disease |
Canavan disease (CAND) [MIM:271900] |
|
rs750670270
|
Disease |
Carbamoyl phosphate synthetase 1 deficiency (CPS1D) [MIM:237300] |
|
rs752339705
|
Disease |
Carbamoyl phosphate synthetase 1 deficiency (CPS1D) [MIM:237300] |
|
rs757205958
|
Disease |
Carbamoyl phosphate synthetase 1 deficiency (CPS1D) [MIM:237300] |
|
rs761064915
|
Disease |
Canavan disease (CAND) [MIM:271900] |
|
rs765561257
|
Disease |
Succinic semialdehyde dehydrogenase deficiency (SSADHD) [MIM:271980] |
|
rs768215008
|
Disease |
Citrullinemia 1 (CTLN1) [MIM:215700] |
|
rs769018733
|
Disease |
Citrullinemia 1 (CTLN1) [MIM:215700] |
|
rs773049803
|
Disease |
Canavan disease (CAND) [MIM:271900] |
|
rs774323189
|
Disease |
Canavan disease (CAND) [MIM:271900] |
|
rs775163147
|
Disease |
Citrullinemia 1 (CTLN1) [MIM:215700] |
|
rs775305020
|
Disease |
Citrullinemia 1 (CTLN1) [MIM:215700] |
|
rs776777887
|
Disease |
Canavan disease (CAND) [MIM:271900] |
|
rs777233486
|
Disease |
Carbamoyl phosphate synthetase 1 deficiency (CPS1D) [MIM:237300] |
|
rs796052061
|
Disease |
Hyperoxaluria primary 1 (HP1) [MIM:259900] |
|
rs80358214
|
Disease |
Congenital systemic glutamine deficiency (CSGD) [MIM:610015] |
|
rs933813349
|
Disease |
Carbamoyl phosphate synthetase 1 deficiency (CPS1D) [MIM:237300] |
|
rs936192871
|
Disease |
Citrullinemia 1 (CTLN1) [MIM:215700] |
|
rs937670540
|
Disease |
Canavan disease (CAND) [MIM:271900] |
|
rn00254
|
Aflatoxin biosynthesis
|
|
dbSNP |
Type |
Disease name |
|
rs1357271377
|
Unclassified |
A colorectal cancer sample |
|
hsa00260
|
Glycine, serine and threonine metabolism
|
|
dbSNP |
Type |
Disease name |
|
-
|
Disease |
Cystathionine beta-synthase deficiency (CBSD) [MIM:236200] |
|
-
|
Disease |
Cerebral creatine deficiency syndrome 2 (CCDS2) [MIM:612736] |
|
rs1041969
|
Polymorphism |
- |
|
rs104894035
|
Disease |
Phosphoserine phosphatase deficiency (PSPHD) [MIM:614023] |
|
rs104894036
|
Disease |
Phosphoserine phosphatase deficiency (PSPHD) [MIM:614023] |
|
rs104894694
|
Disease |
Cerebral creatine deficiency syndrome 2 (CCDS2) [MIM:612736] |
|
rs115014558
|
Polymorphism |
- |
|
rs1170128038
|
Disease |
Cystathionine beta-synthase deficiency (CBSD) [MIM:236200] |
|
rs1191141364
|
Disease |
Cystathionine beta-synthase deficiency (CBSD) [MIM:236200] |
|
rs121908520
|
Disease |
Hyperoxaluria primary 1 (HP1) [MIM:259900] |
|
rs121908524
|
Disease |
Hyperoxaluria primary 1 (HP1) [MIM:259900] |
|
rs121908527
|
Disease |
Hyperoxaluria primary 1 (HP1) [MIM:259900] |
|
rs121908530
|
Disease |
Hyperoxaluria primary 1 (HP1) [MIM:259900] |
|
rs121912707
|
Disease |
Pyridoxine-dependent epilepsy (PDE) [MIM:266100] |
|
rs121912711
|
Disease |
Pyridoxine-dependent epilepsy (PDE) [MIM:266100] |
|
rs121964925
|
Disease |
Erythrocytosis, familial, 8 (ECYT8) [MIM:222800] |
|
rs121964962
|
Disease |
Cystathionine beta-synthase deficiency (CBSD) [MIM:236200] |
|
rs121964969
|
Disease |
Cystathionine beta-synthase deficiency (CBSD) [MIM:236200] |
|
rs121964972
|
Disease |
Cystathionine beta-synthase deficiency (CBSD) [MIM:236200] |
|
rs121964988
|
Disease |
Dihydrolipoamide dehydrogenase deficiency (DLDD) [MIM:246900] |
|
rs121964991
|
Disease |
Dihydrolipoamide dehydrogenase deficiency (DLDD) [MIM:246900] |
|
rs121964993
|
Disease |
Dihydrolipoamide dehydrogenase deficiency (DLDD) [MIM:246900] |
|
rs1229984
|
Polymorphism |
- |
|
rs13408961
|
Polymorphism |
- |
|
rs1371496558
|
Disease |
Cerebral creatine deficiency syndrome 2 (CCDS2) [MIM:612736] |
|
rs140778208
|
Polymorphism |
- |
|
rs140992177
|
Polymorphism |
- |
|
rs142814307
|
Disease |
Cerebral creatine deficiency syndrome 3 (CCDS3) [MIM:612718] |
|
rs1441030187
|
Disease |
Cerebral creatine deficiency syndrome 2 (CCDS2) [MIM:612736] |
|
rs1447665588
|
Disease |
Cerebral creatine deficiency syndrome 2 (CCDS2) [MIM:612736] |
|
rs148865119
|
Disease |
Cystathionine beta-synthase deficiency (CBSD) [MIM:236200] |
|
rs150338273
|
Polymorphism |
- |
|
rs1555874803
|
Disease |
Cystathionine beta-synthase deficiency (CBSD) [MIM:236200] |
|
rs180177155
|
Disease |
Hyperoxaluria primary 1 (HP1) [MIM:259900] |
|
rs180177156
|
Disease |
Hyperoxaluria primary 1 (HP1) [MIM:259900] |
|
rs180177157
|
Disease |
Hyperoxaluria primary 1 (HP1) [MIM:259900] |
|
rs180177173
|
Disease |
Hyperoxaluria primary 1 (HP1) [MIM:259900] |
|
rs180177185
|
Disease |
Hyperoxaluria primary 1 (HP1) [MIM:259900] |
|
rs180177197
|
Disease |
Hyperoxaluria primary 1 (HP1) [MIM:259900] |
|
rs180177225
|
Disease |
Hyperoxaluria primary 1 (HP1) [MIM:259900] |
|
rs180177236
|
Disease |
Hyperoxaluria primary 1 (HP1) [MIM:259900] |
|
rs180177244
|
Disease |
Hyperoxaluria primary 1 (HP1) [MIM:259900] |
|
rs180177253
|
Disease |
Hyperoxaluria primary 1 (HP1) [MIM:259900] |
|
rs180177264
|
Disease |
Hyperoxaluria primary 1 (HP1) [MIM:259900] |
|
rs180177289
|
Disease |
Hyperoxaluria primary 1 (HP1) [MIM:259900] |
|
rs180177290
|
Disease |
Hyperoxaluria primary 1 (HP1) [MIM:259900] |
|
rs200833152
|
Polymorphism |
- |
|
rs2066702
|
Polymorphism |
- |
|
rs267606947
|
Disease |
Phosphoglycerate dehydrogenase deficiency (PHGDHD) [MIM:601815] |
|
rs267606949
|
Disease |
Phosphoglycerate dehydrogenase deficiency (PHGDHD) [MIM:601815] |
|
rs28730628
|
Polymorphism |
- |
|
rs28941786
|
Disease |
Cystathioninuria (CSTNU) [MIM:219500] |
|
rs34885252
|
Polymorphism |
- |
|
rs35385902
|
Polymorphism |
- |
|
rs372027428
|
Polymorphism |
- |
|
rs376982466
|
Disease |
Cerebral creatine deficiency syndrome 3 (CCDS3) [MIM:612718] |
|
rs377578020
|
Disease |
Cerebral creatine deficiency syndrome 3 (CCDS3) [MIM:612718] |
|
rs4426527
|
Polymorphism |
- |
|
rs555959266
|
Disease |
Cystathionine beta-synthase deficiency (CBSD) [MIM:236200] |
|
rs73106685
|
Polymorphism |
- |
|
rs751972865
|
Disease |
Erythrocytosis, familial, 8 (ECYT8) [MIM:222800] |
|
rs755952006
|
Disease |
Cystathionine beta-synthase deficiency (CBSD) [MIM:236200] |
|
rs758236584
|
Disease |
Cystathionine beta-synthase deficiency (CBSD) [MIM:236200] |
|
rs760214620
|
Disease |
Cystathionine beta-synthase deficiency (CBSD) [MIM:236200] |
|
rs761647392
|
Disease |
Cystathionine beta-synthase deficiency (CBSD) [MIM:236200] |
|
rs762065361
|
Disease |
Cystathionine beta-synthase deficiency (CBSD) [MIM:236200] |
|
rs763835246
|
Disease |
Cystathionine beta-synthase deficiency (CBSD) [MIM:236200] |
|
rs771298943
|
Disease |
Cystathionine beta-synthase deficiency (CBSD) [MIM:236200] |
|
rs773734233
|
Disease |
Cystathionine beta-synthase deficiency (CBSD) [MIM:236200] |
|
rs774144200
|
Disease |
Cerebral creatine deficiency syndrome 2 (CCDS2) [MIM:612736] |
|
rs779270933
|
Disease |
Cystathionine beta-synthase deficiency (CBSD) [MIM:236200] |
|
rs796052061
|
Disease |
Hyperoxaluria primary 1 (HP1) [MIM:259900] |
|
rs80338734
|
Disease |
Cerebral creatine deficiency syndrome 2 (CCDS2) [MIM:612736] |
|
rs864321678
|
Disease |
Glycine N-methyltransferase deficiency (GNMT deficiency) [MIM:606664] |
|
hsa00270
|
Cysteine and methionine metabolism
|
|
dbSNP |
Type |
Disease name |
|
-
|
Disease |
Cystathionine beta-synthase deficiency (CBSD) [MIM:236200] |
|
rs1170128038
|
Disease |
Cystathionine beta-synthase deficiency (CBSD) [MIM:236200] |
|
rs1191141364
|
Disease |
Cystathionine beta-synthase deficiency (CBSD) [MIM:236200] |
|
rs121964962
|
Disease |
Cystathionine beta-synthase deficiency (CBSD) [MIM:236200] |
|
rs121964963
|
Disease |
Cystathionine beta-synthase deficiency (CBSD) [MIM:236200] |
|
rs121964966
|
Disease |
Cystathionine beta-synthase deficiency (CBSD) [MIM:236200] |
|
rs121964968
|
Disease |
Cystathionine beta-synthase deficiency (CBSD) [MIM:236200] |
|
rs121964969
|
Disease |
Cystathionine beta-synthase deficiency (CBSD) [MIM:236200] |
|
rs121964972
|
Disease |
Cystathionine beta-synthase deficiency (CBSD) [MIM:236200] |
|
rs1347651454
|
Disease |
Cystathionine beta-synthase deficiency (CBSD) [MIM:236200] |
|
rs1555874803
|
Disease |
Cystathionine beta-synthase deficiency (CBSD) [MIM:236200] |
|
rs267606947
|
Disease |
Phosphoglycerate dehydrogenase deficiency (PHGDHD) [MIM:601815] |
|
rs267606949
|
Disease |
Phosphoglycerate dehydrogenase deficiency (PHGDHD) [MIM:601815] |
|
rs267607076
|
Disease |
X-linked syndromic mental retardation Snyder-Robinson type (MRXSSR) [MIM:309583] |
|
rs28941786
|
Disease |
Cystathioninuria (CSTNU) [MIM:219500] |
|
rs373782713
|
Disease |
Cystathionine beta-synthase deficiency (CBSD) [MIM:236200] |
|
rs555959266
|
Disease |
Cystathionine beta-synthase deficiency (CBSD) [MIM:236200] |
|
rs755106884
|
Disease |
Cystathionine beta-synthase deficiency (CBSD) [MIM:236200] |
|
rs755952006
|
Disease |
Cystathionine beta-synthase deficiency (CBSD) [MIM:236200] |
|
rs758236584
|
Disease |
Cystathionine beta-synthase deficiency (CBSD) [MIM:236200] |
|
rs760214620
|
Disease |
Cystathionine beta-synthase deficiency (CBSD) [MIM:236200] |
|
rs761647392
|
Disease |
Cystathionine beta-synthase deficiency (CBSD) [MIM:236200] |
|
rs762065361
|
Disease |
Cystathionine beta-synthase deficiency (CBSD) [MIM:236200] |
|
rs763835246
|
Disease |
Cystathionine beta-synthase deficiency (CBSD) [MIM:236200] |
|
rs771298943
|
Disease |
Cystathionine beta-synthase deficiency (CBSD) [MIM:236200] |
|
rs773734233
|
Disease |
Cystathionine beta-synthase deficiency (CBSD) [MIM:236200] |
|
rs777954556
|
Disease |
Lactate dehydrogenase B deficiency (LDHBD) [MIM:614128] |
|
rs779270933
|
Disease |
Cystathionine beta-synthase deficiency (CBSD) [MIM:236200] |
|
rs782308462
|
Disease |
Epileptic encephalopathy, early infantile, 51 (EIEE51) [MIM:617339] |
|
hsa00280
|
Valine, leucine and isoleucine degradation
|
|
dbSNP |
Type |
Disease name |
|
-
|
Disease |
Succinyl-CoA:3-oxoacid CoA transferase deficiency (SCOTD) [MIM:245050] |
|
-
|
Disease |
3-hydroxy-3-methylglutaryl-CoA lyase deficiency (HMGCLD) [MIM:246450] |
|
rs104886492
|
Unclassified |
HDS10 mitochondrial disease (HSD10MD) [MIM:300438] |
|
rs120074140
|
Disease |
3-ketothiolase deficiency (3KTD) [MIM:203750] |
|
rs120074141
|
Disease |
3-ketothiolase deficiency (3KTD) [MIM:203750] |
|
rs120074146
|
Disease |
3-ketothiolase deficiency (3KTD) [MIM:203750] |
|
rs120074147
|
Disease |
3-ketothiolase deficiency (3KTD) [MIM:203750] |
|
rs121434275
|
Disease |
Acyl-CoA dehydrogenase medium-chain deficiency (ACADMD) [MIM:201450] |
|
rs121434278
|
Disease |
Acyl-CoA dehydrogenase medium-chain deficiency (ACADMD) [MIM:201450] |
|
rs121434279
|
Disease |
Acyl-CoA dehydrogenase medium-chain deficiency (ACADMD) [MIM:201450] |
|
rs121434281
|
Disease |
Acyl-CoA dehydrogenase medium-chain deficiency (ACADMD) [MIM:201450] |
|
rs121434283
|
Disease |
Acyl-CoA dehydrogenase medium-chain deficiency (ACADMD) [MIM:201450] |
|
rs121909301
|
Disease |
Succinyl-CoA:3-oxoacid CoA transferase deficiency (SCOTD) [MIM:245050] |
|
rs121912707
|
Disease |
Pyridoxine-dependent epilepsy (PDE) [MIM:266100] |
|
rs121912711
|
Disease |
Pyridoxine-dependent epilepsy (PDE) [MIM:266100] |
|
rs121918329
|
Disease |
3-hydroxyisobutryl-CoA hydrolase deficiency (HIBCHD) [MIM:250620] |
|
rs121964988
|
Disease |
Dihydrolipoamide dehydrogenase deficiency (DLDD) [MIM:246900] |
|
rs121964991
|
Disease |
Dihydrolipoamide dehydrogenase deficiency (DLDD) [MIM:246900] |
|
rs121964993
|
Disease |
Dihydrolipoamide dehydrogenase deficiency (DLDD) [MIM:246900] |
|
rs1327401976
|
Disease |
Succinyl-CoA:3-oxoacid CoA transferase deficiency (SCOTD) [MIM:245050] |
|
rs1357271377
|
Unclassified |
A colorectal cancer sample |
|
rs1357942068
|
Disease |
3-hydroxy-3-methylglutaryl-CoA lyase deficiency (HMGCLD) [MIM:246450] |
|
rs137852640
|
Disease |
3-hydroxy-3-methylglutaryl-CoA synthase-2 deficiency (HMGCS2D) [MIM:605911] |
|
rs137853096
|
Disease |
D-bifunctional protein deficiency (DBPD) [MIM:261515] |
|
rs137853101
|
Disease |
3-alpha-hydroxyacyl-CoA dehydrogenase deficiency (HADH deficiency) [MIM:231530] |
|
rs137853102
|
Disease |
3-alpha-hydroxyacyl-CoA dehydrogenase deficiency (HADH deficiency) [MIM:231530] |
|
rs141786030
|
Polymorphism |
- |
|
rs1420321267
|
Disease |
3-ketothiolase deficiency (3KTD) [MIM:203750] |
|
rs148639841
|
Disease |
3-ketothiolase deficiency (3KTD) [MIM:203750] |
|
rs1553131940
|
Disease |
3-hydroxy-3-methylglutaryl-CoA lyase deficiency (HMGCLD) [MIM:246450] |
|
rs182923857
|
Disease |
Maple syrup urine disease 1A (MSUD1A) [MIM:248600] |
|
rs199587895
|
Disease |
3-hydroxy-3-methylglutaryl-CoA lyase deficiency (HMGCLD) [MIM:246450] |
|
rs398123503
|
Disease |
Maple syrup urine disease 1A (MSUD1A) [MIM:248600] |
|
rs56199635
|
Polymorphism |
- |
|
rs727503963
|
Disease |
3-hydroxy-3-methylglutaryl-CoA lyase deficiency (HMGCLD) [MIM:246450] |
|
rs760106433
|
Disease |
3-hydroxy-3-methylglutaryl-CoA lyase deficiency (HMGCLD) [MIM:246450] |
|
rs769688327
|
Disease |
Maple syrup urine disease 1A (MSUD1A) [MIM:248600] |
|
rs769894315
|
Disease |
3-methylglutaconic aciduria 1 (MGA1) [MIM:250950] |
|
rs886041122
|
Disease |
3-ketothiolase deficiency (3KTD) [MIM:203750] |
|
rn00281
|
Geraniol degradation
|
|
dbSNP |
Type |
Disease name |
|
rs104886492
|
Unclassified |
HDS10 mitochondrial disease (HSD10MD) [MIM:300438] |
|
rs137853096
|
Disease |
D-bifunctional protein deficiency (DBPD) [MIM:261515] |
|
rs137853101
|
Disease |
3-alpha-hydroxyacyl-CoA dehydrogenase deficiency (HADH deficiency) [MIM:231530] |
|
rs137853102
|
Disease |
3-alpha-hydroxyacyl-CoA dehydrogenase deficiency (HADH deficiency) [MIM:231530] |
|
rn00300
|
Lysine biosynthesis
|
|
dbSNP |
Type |
Disease name |
|
rs121912707
|
Disease |
Pyridoxine-dependent epilepsy (PDE) [MIM:266100] |
|
rs121912711
|
Disease |
Pyridoxine-dependent epilepsy (PDE) [MIM:266100] |
|
hsa00310
|
Lysine degradation
|
|
dbSNP |
Type |
Disease name |
|
-
|
Disease |
Sotos syndrome 1 (SOTOS1) [MIM:117550] |
|
-
|
Disease |
Weaver syndrome (WVS) [MIM:277590] |
|
rs104886492
|
Unclassified |
HDS10 mitochondrial disease (HSD10MD) [MIM:300438] |
|
rs1057519904
|
Disease |
Glioma (GLM) [MIM:137800] |
|
rs120074141
|
Disease |
3-ketothiolase deficiency (3KTD) [MIM:203750] |
|
rs121912707
|
Disease |
Pyridoxine-dependent epilepsy (PDE) [MIM:266100] |
|
rs121912711
|
Disease |
Pyridoxine-dependent epilepsy (PDE) [MIM:266100] |
|
rs121964988
|
Disease |
Dihydrolipoamide dehydrogenase deficiency (DLDD) [MIM:246900] |
|
rs121964991
|
Disease |
Dihydrolipoamide dehydrogenase deficiency (DLDD) [MIM:246900] |
|
rs121964993
|
Disease |
Dihydrolipoamide dehydrogenase deficiency (DLDD) [MIM:246900] |
|
rs137853096
|
Disease |
D-bifunctional protein deficiency (DBPD) [MIM:261515] |
|
rs137853101
|
Disease |
3-alpha-hydroxyacyl-CoA dehydrogenase deficiency (HADH deficiency) [MIM:231530] |
|
rs137853102
|
Disease |
3-alpha-hydroxyacyl-CoA dehydrogenase deficiency (HADH deficiency) [MIM:231530] |
|
rs1478147351
|
Unclassified |
Leukemia, acute lymphoblastic (ALL) [MIM:613065] |
|
rs1555028104
|
Unclassified |
Mental retardation, autosomal dominant 51 (MRD51) [MIM:617788] |
|
rs1740231
|
Polymorphism |
- |
|
rs193921147
|
Disease |
Weaver syndrome (WVS) [MIM:277590] |
|
rs267601394
|
Polymorphism |
- |
|
rs587783625
|
Unclassified |
Weaver syndrome (WVS) [MIM:277590] |
|
rs587784176
|
Disease |
Sotos syndrome 1 (SOTOS1) [MIM:117550] |
|
rs797045825
|
Disease |
Sotos syndrome 1 (SOTOS1) [MIM:117550] |
|
hsa00330
|
Arginine and proline metabolism
|
|
dbSNP |
Type |
Disease name |
|
-
|
Disease |
Argininemia (ARGIN) [MIM:207800] |
|
-
|
Disease |
Cerebral creatine deficiency syndrome 2 (CCDS2) [MIM:612736] |
|
rs104893943
|
Disease |
Argininemia (ARGIN) [MIM:207800] |
|
rs104894694
|
Disease |
Cerebral creatine deficiency syndrome 2 (CCDS2) [MIM:612736] |
|
rs121434583
|
Disease |
Cutis laxa, autosomal recessive, 3A (ARCL3A) [MIM:219150] |
|
rs121912707
|
Disease |
Pyridoxine-dependent epilepsy (PDE) [MIM:266100] |
|
rs121912711
|
Disease |
Pyridoxine-dependent epilepsy (PDE) [MIM:266100] |
|
rs1371496558
|
Disease |
Cerebral creatine deficiency syndrome 2 (CCDS2) [MIM:612736] |
|
rs137852937
|
Disease |
Hyperprolinemia 2 (HYRPRO2) [MIM:239510] |
|
rs138207257
|
Disease |
Hyperoxaluria primary 3 (HP3) [MIM:613616] |
|
rs13894
|
Polymorphism |
- |
|
rs139751598
|
Disease |
Cutis laxa, autosomal recessive, 2B (ARCL2B) [MIM:612940] |
|
rs140778208
|
Polymorphism |
- |
|
rs142814307
|
Disease |
Cerebral creatine deficiency syndrome 3 (CCDS3) [MIM:612718] |
|
rs1441030187
|
Disease |
Cerebral creatine deficiency syndrome 2 (CCDS2) [MIM:612736] |
|
rs1447665588
|
Disease |
Cerebral creatine deficiency syndrome 2 (CCDS2) [MIM:612736] |
|
rs150338273
|
Polymorphism |
- |
|
rs200833152
|
Polymorphism |
- |
|
rs267607076
|
Disease |
X-linked syndromic mental retardation Snyder-Robinson type (MRXSSR) [MIM:309583] |
|
rs372027428
|
Polymorphism |
- |
|
rs376982466
|
Disease |
Cerebral creatine deficiency syndrome 3 (CCDS3) [MIM:612718] |
|
rs377578020
|
Disease |
Cerebral creatine deficiency syndrome 3 (CCDS3) [MIM:612718] |
|
rs752669339
|
Disease |
Spastic paraplegia 9B, autosomal recessive (SPG9B) [MIM:616586] |
|
rs766264810
|
Disease |
Spastic paraplegia 9A, autosomal dominant (SPG9A) [MIM:601162] |
|
rs774047299
|
Disease |
Cutis laxa, autosomal recessive, 3A (ARCL3A) [MIM:219150] |
|
rs774144200
|
Disease |
Cerebral creatine deficiency syndrome 2 (CCDS2) [MIM:612736] |
|
rs80338734
|
Disease |
Cerebral creatine deficiency syndrome 2 (CCDS2) [MIM:612736] |
|
rs869320690
|
Disease |
Spastic paraplegia 9B, autosomal recessive (SPG9B) [MIM:616586] |
|
rn00332
|
Carbapenem biosynthesis
|
|
dbSNP |
Type |
Disease name |
|
rs121434583
|
Disease |
Cutis laxa, autosomal recessive, 3A (ARCL3A) [MIM:219150] |
|
rs752669339
|
Disease |
Spastic paraplegia 9B, autosomal recessive (SPG9B) [MIM:616586] |
|
rs766264810
|
Disease |
Spastic paraplegia 9A, autosomal dominant (SPG9A) [MIM:601162] |
|
rs774047299
|
Disease |
Cutis laxa, autosomal recessive, 3A (ARCL3A) [MIM:219150] |
|
rs869320690
|
Disease |
Spastic paraplegia 9B, autosomal recessive (SPG9B) [MIM:616586] |
|
hsa00340
|
Histidine metabolism
|
|
dbSNP |
Type |
Disease name |
|
-
|
Disease |
Canavan disease (CAND) [MIM:271900] |
|
-
|
Disease |
Microphthalmia, isolated, 8 (MCOP8) [MIM:615113] |
|
rs1014551540
|
Disease |
Canavan disease (CAND) [MIM:271900] |
|
rs104894550
|
Disease |
Canavan disease (CAND) [MIM:271900] |
|
rs121912707
|
Disease |
Pyridoxine-dependent epilepsy (PDE) [MIM:266100] |
|
rs121912711
|
Disease |
Pyridoxine-dependent epilepsy (PDE) [MIM:266100] |
|
rs1414684396
|
Disease |
Canavan disease (CAND) [MIM:271900] |
|
rs1555538144
|
Disease |
Canavan disease (CAND) [MIM:271900] |
|
rs1555538148
|
Disease |
Canavan disease (CAND) [MIM:271900] |
|
rs1555538151
|
Disease |
Canavan disease (CAND) [MIM:271900] |
|
rs28940279
|
Disease |
Canavan disease (CAND) [MIM:271900] |
|
rs758252808
|
Disease |
Mental retardation, autosomal recessive 51 (MRT51) [MIM:616739] |
|
rs773049803
|
Disease |
Canavan disease (CAND) [MIM:271900] |
|
rs774323189
|
Disease |
Canavan disease (CAND) [MIM:271900] |
|
rs776777887
|
Disease |
Canavan disease (CAND) [MIM:271900] |
|
rs777936704
|
Disease |
Canavan disease (CAND) [MIM:271900] |
|
rs937670540
|
Disease |
Canavan disease (CAND) [MIM:271900] |
|
hsa00350
|
Tyrosine metabolism
|
|
dbSNP |
Type |
Disease name |
|
-
|
Disease |
Succinic semialdehyde dehydrogenase deficiency (SSADHD) [MIM:271980] |
|
-
|
Disease |
Tyrosinemia 3 (TYRSN3) [MIM:276710] |
|
-
|
Disease |
Microphthalmia, isolated, 8 (MCOP8) [MIM:615113] |
|
rs1041969
|
Polymorphism |
- |
|
rs1229984
|
Polymorphism |
- |
|
rs1326526453
|
Disease |
Succinic semialdehyde dehydrogenase deficiency (SSADHD) [MIM:271980] |
|
rs137852865
|
Disease |
Tyrosinemia 3 (TYRSN3) [MIM:276710] |
|
rs145087265
|
Disease |
Succinic semialdehyde dehydrogenase deficiency (SSADHD) [MIM:271980] |
|
rs2066702
|
Polymorphism |
- |
|
rs267606760
|
Disease |
Orthostatic hypotension 1 (ORTHYP1) [MIM:223360] |
|
rs28730628
|
Polymorphism |
- |
|
rs35097308
|
Polymorphism |
- |
|
rs35385902
|
Polymorphism |
- |
|
rs375628463
|
Disease |
Succinic semialdehyde dehydrogenase deficiency (SSADHD) [MIM:271980] |
|
rs408038
|
Polymorphism |
- |
|
rs4986871
|
Polymorphism |
- |
|
rs5319
|
Polymorphism |
- |
|
rs5639
|
Polymorphism |
- |
|
rs5641
|
Polymorphism |
- |
|
rs62621664
|
Polymorphism |
- |
|
rs72552283
|
Disease |
Succinic semialdehyde dehydrogenase deficiency (SSADHD) [MIM:271980] |
|
rs765561257
|
Disease |
Succinic semialdehyde dehydrogenase deficiency (SSADHD) [MIM:271980] |
|
hsa00360
|
Phenylalanine metabolism
|
|
dbSNP |
Type |
Disease name |
|
-
|
Disease |
Phenylketonuria (PKU) [MIM:261600] |
|
-
|
Disease |
Tyrosinemia 3 (TYRSN3) [MIM:276710] |
|
-
|
Disease |
Microphthalmia, isolated, 8 (MCOP8) [MIM:615113] |
|
rs1041969
|
Polymorphism |
- |
|
rs104886492
|
Unclassified |
HDS10 mitochondrial disease (HSD10MD) [MIM:300438] |
|
rs118203925
|
Disease |
Non-phenylketonuria hyperphenylalaninemia (Non-PKU HPA) [MIM:261600] |
|
rs1229984
|
Polymorphism |
- |
|
rs137852865
|
Disease |
Tyrosinemia 3 (TYRSN3) [MIM:276710] |
|
rs137853096
|
Disease |
D-bifunctional protein deficiency (DBPD) [MIM:261515] |
|
rs137853101
|
Disease |
3-alpha-hydroxyacyl-CoA dehydrogenase deficiency (HADH deficiency) [MIM:231530] |
|
rs137853102
|
Disease |
3-alpha-hydroxyacyl-CoA dehydrogenase deficiency (HADH deficiency) [MIM:231530] |
|
rs1486763160
|
Disease |
Phenylketonuria (PKU) [MIM:261600] |
|
rs199475567
|
Disease |
Phenylketonuria (PKU) [MIM:261600] |
|
rs199475579
|
Disease |
Phenylketonuria (PKU) [MIM:261600] |
|
rs199475580
|
Disease |
Phenylketonuria (PKU) [MIM:261600] |
|
rs199475582
|
Disease |
Phenylketonuria (PKU) [MIM:261600] |
|
rs199475598
|
Disease |
Hyperphenylalaninemia (HPA) [MIM:261600] |
|
rs199475610
|
Disease |
Phenylketonuria (PKU) [MIM:261600] |
|
rs199475643
|
Disease |
Hyperphenylalaninemia (HPA) [MIM:261600] |
|
rs199475651
|
Disease |
Phenylketonuria (PKU) [MIM:261600] |
|
rs2066702
|
Polymorphism |
- |
|
rs28730628
|
Polymorphism |
- |
|
rs35385902
|
Polymorphism |
- |
|
rs35670089
|
Polymorphism |
- |
|
rs35702888
|
Polymorphism |
- |
|
rs5030841
|
Disease |
Phenylketonuria (PKU) [MIM:261600] |
|
rs5030842
|
Disease |
Phenylketonuria (PKU) [MIM:261600] |
|
rs5030847
|
Disease |
Phenylketonuria (PKU) [MIM:261600] |
|
rs5030851
|
Disease |
Phenylketonuria (PKU) [MIM:261600] |
|
rs62507340
|
Disease |
Phenylketonuria (PKU) [MIM:261600] |
|
rs62507347
|
Disease |
Non-phenylketonuria hyperphenylalaninemia (Non-PKU HPA) [MIM:261600] |
|
rs62508578
|
Disease |
Phenylketonuria (PKU) [MIM:261600] |
|
rs62508580
|
Disease |
Phenylketonuria (PKU) [MIM:261600] |
|
rs62508588
|
Disease |
Non-phenylketonuria hyperphenylalaninemia (Non-PKU HPA) [MIM:261600] |
|
rs62508694
|
Disease |
Phenylketonuria (PKU) [MIM:261600] |
|
rs62508698
|
Disease |
Phenylketonuria (PKU) [MIM:261600] |
|
rs62514902
|
Disease |
Phenylketonuria (PKU) [MIM:261600] |
|
rs62514958
|
Disease |
Phenylketonuria (PKU) [MIM:261600] |
|
rs62516062
|
Disease |
Phenylketonuria (PKU) [MIM:261600] |
|
rs62517181
|
Disease |
Phenylketonuria (PKU) [MIM:261600] |
|
rs62635346
|
Disease |
Phenylketonuria (PKU) [MIM:261600] |
|
rs62642916
|
Disease |
Phenylketonuria (PKU) [MIM:261600] |
|
rs62642918
|
Disease |
Phenylketonuria (PKU) [MIM:261600] |
|
rs62642930
|
Disease |
Phenylketonuria (PKU) [MIM:261600] |
|
rs62642934
|
Disease |
Non-phenylketonuria hyperphenylalaninemia (Non-PKU HPA) [MIM:261600] |
|
rs62642942
|
Disease |
Phenylketonuria (PKU) [MIM:261600] |
|
rs62642944
|
Disease |
Phenylketonuria (PKU) [MIM:261600] |
|
rs74503222
|
Disease |
Phenylketonuria (PKU) [MIM:261600] |
|
rs74603784
|
Disease |
Phenylketonuria (PKU) [MIM:261600] |
|
rs76394784
|
Disease |
Phenylketonuria (PKU) [MIM:261600] |
|
rn00362
|
Benzoate degradation
|
|
dbSNP |
Type |
Disease name |
|
rs1041969
|
Polymorphism |
- |
|
rs104886492
|
Unclassified |
HDS10 mitochondrial disease (HSD10MD) [MIM:300438] |
|
rs120074141
|
Disease |
3-ketothiolase deficiency (3KTD) [MIM:203750] |
|
rs1229984
|
Polymorphism |
- |
|
rs137853096
|
Disease |
D-bifunctional protein deficiency (DBPD) [MIM:261515] |
|
rs137853101
|
Disease |
3-alpha-hydroxyacyl-CoA dehydrogenase deficiency (HADH deficiency) [MIM:231530] |
|
rs137853102
|
Disease |
3-alpha-hydroxyacyl-CoA dehydrogenase deficiency (HADH deficiency) [MIM:231530] |
|
rs2066702
|
Polymorphism |
- |
|
rs28730628
|
Polymorphism |
- |
|
rs35385902
|
Polymorphism |
- |
|
hsa00380
|
Tryptophan metabolism
|
|
dbSNP |
Type |
Disease name |
|
-
|
Disease |
Glaucoma 3, primary congenital, A (GLC3A) [MIM:231300] |
|
rs1041988
|
Polymorphism |
- |
|
rs104886492
|
Unclassified |
HDS10 mitochondrial disease (HSD10MD) [MIM:300438] |
|
rs104893628
|
Disease |
Glaucoma 3, primary congenital, A (GLC3A) [MIM:231300] |
|
rs120074141
|
Disease |
3-ketothiolase deficiency (3KTD) [MIM:203750] |
|
rs121912707
|
Disease |
Pyridoxine-dependent epilepsy (PDE) [MIM:266100] |
|
rs121912711
|
Disease |
Pyridoxine-dependent epilepsy (PDE) [MIM:266100] |
|
rs121918822
|
Polymorphism |
- |
|
rs121918823
|
Polymorphism |
- |
|
rs121918824
|
Polymorphism |
- |
|
rs121964988
|
Disease |
Dihydrolipoamide dehydrogenase deficiency (DLDD) [MIM:246900] |
|
rs121964991
|
Disease |
Dihydrolipoamide dehydrogenase deficiency (DLDD) [MIM:246900] |
|
rs121964993
|
Disease |
Dihydrolipoamide dehydrogenase deficiency (DLDD) [MIM:246900] |
|
rs12721627
|
Polymorphism |
- |
|
rs12721629
|
Polymorphism |
- |
|
rs137853096
|
Disease |
D-bifunctional protein deficiency (DBPD) [MIM:261515] |
|
rs137853101
|
Disease |
3-alpha-hydroxyacyl-CoA dehydrogenase deficiency (HADH deficiency) [MIM:231530] |
|
rs137853102
|
Disease |
3-alpha-hydroxyacyl-CoA dehydrogenase deficiency (HADH deficiency) [MIM:231530] |
|
rs148036160
|
Polymorphism |
- |
|
rs148542782
|
Disease |
Glaucoma 3, primary congenital, A (GLC3A) [MIM:231300] |
|
rs1553957997
|
Disease |
Hypertryptophanemia (HYPTRP) [MIM:600627] |
|
rs17110563
|
Polymorphism |
- |
|
rs201316181
|
Polymorphism |
- |
|
rs2302339
|
Polymorphism |
- |
|
rs28936701
|
Disease |
Glaucoma 3, primary congenital, A (GLC3A) [MIM:231300] |
|
rs373339042
|
Polymorphism |
- |
|
rs4986910
|
Polymorphism |
- |
|
rs4987161
|
Polymorphism |
- |
|
rs55785340
|
Polymorphism |
- |
|
rs55901263
|
Polymorphism |
- |
|
rs55951658
|
Polymorphism |
- |
|
rs55989760
|
Disease |
Glaucoma 3, primary congenital, A (GLC3A) [MIM:231300] |
|
rs56324128
|
Polymorphism |
- |
|
rs56800285
|
Polymorphism |
- |
|
rs66583685
|
Disease |
Glaucoma 3, primary congenital, A (GLC3A) [MIM:231300] |
|
rs67784355
|
Polymorphism |
- |
|
rs6970210
|
Polymorphism |
- |
|
rs72549378
|
Disease |
Glaucoma 3, primary congenital, A (GLC3A) [MIM:231300] |
|
rs72552799
|
Polymorphism |
- |
|
rs752456881
|
Polymorphism |
- |
|
rs9282670
|
Polymorphism |
- |
|
hsa00400
|
Phenylalanine, tyrosine and tryptophan biosynthesis
|
|
dbSNP |
Type |
Disease name |
|
-
|
Disease |
Phenylketonuria (PKU) [MIM:261600] |
|
rs118203925
|
Disease |
Non-phenylketonuria hyperphenylalaninemia (Non-PKU HPA) [MIM:261600] |
|
rs1486763160
|
Disease |
Phenylketonuria (PKU) [MIM:261600] |
|
rs199475567
|
Disease |
Phenylketonuria (PKU) [MIM:261600] |
|
rs199475579
|
Disease |
Phenylketonuria (PKU) [MIM:261600] |
|
rs199475580
|
Disease |
Phenylketonuria (PKU) [MIM:261600] |
|
rs199475582
|
Disease |
Phenylketonuria (PKU) [MIM:261600] |
|
rs199475598
|
Disease |
Hyperphenylalaninemia (HPA) [MIM:261600] |
|
rs199475610
|
Disease |
Phenylketonuria (PKU) [MIM:261600] |
|
rs199475643
|
Disease |
Hyperphenylalaninemia (HPA) [MIM:261600] |
|
rs199475651
|
Disease |
Phenylketonuria (PKU) [MIM:261600] |
|
rs5030841
|
Disease |
Phenylketonuria (PKU) [MIM:261600] |
|
rs5030842
|
Disease |
Phenylketonuria (PKU) [MIM:261600] |
|
rs5030847
|
Disease |
Phenylketonuria (PKU) [MIM:261600] |
|
rs5030851
|
Disease |
Phenylketonuria (PKU) [MIM:261600] |
|
rs62507340
|
Disease |
Phenylketonuria (PKU) [MIM:261600] |
|
rs62507347
|
Disease |
Non-phenylketonuria hyperphenylalaninemia (Non-PKU HPA) [MIM:261600] |
|
rs62508578
|
Disease |
Phenylketonuria (PKU) [MIM:261600] |
|
rs62508580
|
Disease |
Phenylketonuria (PKU) [MIM:261600] |
|
rs62508588
|
Disease |
Non-phenylketonuria hyperphenylalaninemia (Non-PKU HPA) [MIM:261600] |
|
rs62508694
|
Disease |
Phenylketonuria (PKU) [MIM:261600] |
|
rs62508698
|
Disease |
Phenylketonuria (PKU) [MIM:261600] |
|
rs62514902
|
Disease |
Phenylketonuria (PKU) [MIM:261600] |
|
rs62514958
|
Disease |
Phenylketonuria (PKU) [MIM:261600] |
|
rs62516062
|
Disease |
Phenylketonuria (PKU) [MIM:261600] |
|
rs62517181
|
Disease |
Phenylketonuria (PKU) [MIM:261600] |
|
rs62635346
|
Disease |
Phenylketonuria (PKU) [MIM:261600] |
|
rs62642916
|
Disease |
Phenylketonuria (PKU) [MIM:261600] |
|
rs62642918
|
Disease |
Phenylketonuria (PKU) [MIM:261600] |
|
rs62642930
|
Disease |
Phenylketonuria (PKU) [MIM:261600] |
|
rs62642934
|
Disease |
Non-phenylketonuria hyperphenylalaninemia (Non-PKU HPA) [MIM:261600] |
|
rs62642942
|
Disease |
Phenylketonuria (PKU) [MIM:261600] |
|
rs62642944
|
Disease |
Phenylketonuria (PKU) [MIM:261600] |
|
rs74503222
|
Disease |
Phenylketonuria (PKU) [MIM:261600] |
|
rs74603784
|
Disease |
Phenylketonuria (PKU) [MIM:261600] |
|
rs76394784
|
Disease |
Phenylketonuria (PKU) [MIM:261600] |
|
hsa00410
|
beta-Alanine metabolism
|
|
dbSNP |
Type |
Disease name |
|
-
|
Disease |
Microphthalmia, isolated, 8 (MCOP8) [MIM:615113] |
|
rs121912707
|
Disease |
Pyridoxine-dependent epilepsy (PDE) [MIM:266100] |
|
rs121912711
|
Disease |
Pyridoxine-dependent epilepsy (PDE) [MIM:266100] |
|
rs121918329
|
Disease |
3-hydroxyisobutryl-CoA hydrolase deficiency (HIBCHD) [MIM:250620] |
|
rs35097308
|
Polymorphism |
- |
|
hsa00430
|
Taurine and hypotaurine metabolism
|
|
dbSNP |
Type |
Disease name |
|
rs1062459
|
Polymorphism |
- |
|
rs1288775
|
Polymorphism |
- |
|
rs142814307
|
Disease |
Cerebral creatine deficiency syndrome 3 (CCDS3) [MIM:612718] |
|
rs147804855
|
Disease |
Cerebral creatine deficiency syndrome 3 (CCDS3) [MIM:612718] |
|
rs377578020
|
Disease |
Cerebral creatine deficiency syndrome 3 (CCDS3) [MIM:612718] |
|
hsa00450
|
Selenocompound metabolism
|
|
dbSNP |
Type |
Disease name |
|
rs28941785
|
Disease |
Cystathioninuria (CSTNU) [MIM:219500] |
|
rs28941786
|
Disease |
Cystathioninuria (CSTNU) [MIM:219500] |
|
rs56350236
|
Polymorphism |
- |
|
rn00460
|
Cyanoamino acid metabolism
|
|
dbSNP |
Type |
Disease name |
|
rs17004876
|
Polymorphism |
- |
|
hsa00471
|
D-Glutamine and D-glutamate metabolism
|
|
dbSNP |
Type |
Disease name |
|
-
|
Disease |
Infantile cataract, skin abnormalities, glutamate excess, and impaired intellectual development (CASGID) [MIM:618339] |
|
hsa00480
|
Glutathione metabolism
|
|
dbSNP |
Type |
Disease name |
|
-
|
Disease |
Glutathione synthetase deficiency (GSS deficiency) [MIM:266130] |
|
-
|
Disease |
Anemia, non-spherocytic hemolytic, due to G6PD deficiency (NSHA) [MIM:300908] |
|
rs1052661
|
Polymorphism |
- |
|
rs1057519906
|
Polymorphism |
- |
|
rs11509436
|
Polymorphism |
- |
|
rs11509438
|
Polymorphism |
- |
|
rs11509439
|
Polymorphism |
- |
|
rs121909308
|
Disease |
Glutathione synthetase deficiency (GSS deficiency) [MIM:266130] |
|
rs121913499
|
Unclassified |
A glioma sample |
|
rs121913502
|
Disease |
D-2-hydroxyglutaric aciduria 2 (D2HGA2) [MIM:613657] |
|
rs137852316
|
Disease |
Anemia, non-spherocytic hemolytic, due to G6PD deficiency (NSHA) [MIM:300908] |
|
rs137852325
|
Disease |
Anemia, non-spherocytic hemolytic, due to G6PD deficiency (NSHA) [MIM:300908] |
|
rs137852329
|
Disease |
Anemia, non-spherocytic hemolytic, due to G6PD deficiency (NSHA) [MIM:300908] |
|
rs137852349
|
Disease |
Anemia, non-spherocytic hemolytic, due to G6PD deficiency (NSHA) [MIM:300908] |
|
rs1695
|
Polymorphism |
- |
|
rs17004876
|
Polymorphism |
- |
|
rs2330837
|
Polymorphism |
- |
|
rs2330838
|
Polymorphism |
- |
|
rs267607076
|
Disease |
X-linked syndromic mental retardation Snyder-Robinson type (MRXSSR) [MIM:309583] |
|
rs28938472
|
Disease |
Glutathione synthetase deficiency (GSS deficiency) [MIM:266130] |
|
rs3895576
|
Polymorphism |
- |
|
rs449856
|
Polymorphism |
- |
|
rs45529437
|
Polymorphism |
- |
|
rs76645461
|
Disease |
Anemia, non-spherocytic hemolytic, due to G6PD deficiency (NSHA) [MIM:300908] |
|
rs78478128
|
Disease |
Anemia, non-spherocytic hemolytic, due to G6PD deficiency (NSHA) [MIM:300908] |
|
rs8177445
|
Polymorphism |
- |
|
rs8190955
|
Polymorphism |
- |
|
rs8190997
|
Polymorphism |
- |
|
hsa00500
|
Starch and sucrose metabolism
|
|
dbSNP |
Type |
Disease name |
|
-
|
Disease |
Maturity-onset diabetes of the young 2 (MODY2) [MIM:125851] |
|
-
|
Disease |
Glycogen storage disease 2 (GSD2) [MIM:232300] |
|
-
|
Disease |
Diabetes mellitus, permanent neonatal (PNDM) [MIM:606176] |
|
-
|
Disease |
Congenital disorder of glycosylation 1T (CDG1T) [MIM:614921] |
|
rs104894009
|
Disease |
Maturity-onset diabetes of the young 2 (MODY2) [MIM:125851] |
|
rs104894015
|
Disease |
Familial hyperinsulinemic hypoglycemia 3 (HHF3) [MIM:602485] |
|
rs1057516600
|
Disease |
Glycogen storage disease 2 (GSD2) [MIM:232300] |
|
rs1131691416
|
Disease |
Maturity-onset diabetes of the young 2 (MODY2) [MIM:125851] |
|
rs113993976
|
Disease |
Glycogen storage disease 6 (GSD6) [MIM:232700] |
|
rs113993977
|
Disease |
Glycogen storage disease 6 (GSD6) [MIM:232700] |
|
rs1270571213
|
Disease |
Interstitial nephritis, karyomegalic (KMIN) [MIM:614817] |
|
rs1286804191
|
Disease |
Diabetes mellitus, permanent neonatal (PNDM) [MIM:606176] |
|
rs1320810473
|
Disease |
Congenital disorder of glycosylation 1T (CDG1T) [MIM:614921] |
|
rs1375656631
|
Disease |
Maturity-onset diabetes of the young 2 (MODY2) [MIM:125851] |
|
rs141533320
|
Disease |
Glycogen storage disease 2 (GSD2) [MIM:232300] |
|
rs142752477
|
Disease |
Glycogen storage disease 2 (GSD2) [MIM:232300] |
|
rs1441649062
|
Disease |
Maturity-onset diabetes of the young 2 (MODY2) [MIM:125851] |
|
rs147065275
|
Disease |
Maturity-onset diabetes of the young 2 (MODY2) [MIM:125851] |
|
rs148311934
|
Disease |
Maturity-onset diabetes of the young 2 (MODY2) [MIM:125851] |
|
rs1554335135
|
Disease |
Maturity-onset diabetes of the young 2 (MODY2) [MIM:125851] |
|
rs1800299
|
Polymorphism |
- |
|
rs193922272
|
Disease |
Maturity-onset diabetes of the young 2 (MODY2) [MIM:125851] |
|
rs193922282
|
Disease |
Diabetes mellitus, permanent neonatal (PNDM) [MIM:606176] |
|
rs193922297
|
Disease |
Maturity-onset diabetes of the young 2 (MODY2) [MIM:125851] |
|
rs193922311
|
Disease |
Maturity-onset diabetes of the young 2 (MODY2) [MIM:125851] |
|
rs368438393
|
Disease |
Glycogen storage disease 2 (GSD2) [MIM:232300] |
|
rs398122379
|
Disease |
Hexokinase deficiency (HK deficiency) [MIM:235700] |
|
rs549029029
|
Disease |
Glycogen storage disease 2 (GSD2) [MIM:232300] |
|
rs751703979
|
Disease |
Interstitial nephritis, karyomegalic (KMIN) [MIM:614817] |
|
rs758737171
|
Disease |
Familial hyperinsulinemic hypoglycemia 3 (HHF3) [MIM:602485] |
|
rs764670084
|
Disease |
Glycogen storage disease 2 (GSD2) [MIM:232300] |
|
rs769268803
|
Disease |
Maturity-onset diabetes of the young 2 (MODY2) [MIM:125851] |
|
rs772883420
|
Disease |
Glycogen storage disease 2 (GSD2) [MIM:232300] |
|
rs80356655
|
Disease |
Maturity-onset diabetes of the young 2 (MODY2) [MIM:125851] |
|
rs80356655
|
Disease |
Diabetes mellitus, permanent neonatal (PNDM) [MIM:606176] |
|
hsa00510
|
N-Glycan biosynthesis
|
|
dbSNP |
Type |
Disease name |
|
rs28934876
|
Disease |
Congenital disorder of glycosylation 1J (CDG1J) [MIM:608093] |
|
rs387906885
|
Disease |
Mental retardation, autosomal recessive 15 (MRT15) [MIM:614202] |
|
rs387906886
|
Disease |
Mental retardation, autosomal recessive 15 (MRT15) [MIM:614202] |
|
rs768464558
|
Disease |
Myasthenic syndrome, congenital, 13 (CMS13) [MIM:614750] |
|
hsa00513
|
Various types of N-glycan biosynthesis
|
|
dbSNP |
Type |
Disease name |
|
-
|
Disease |
GM2-gangliosidosis 1 (GM2G1) [MIM:272800] |
|
rs1054374
|
Polymorphism |
- |
|
rs1131691007
|
Unclassified |
Sporadic cancers |
|
rs1555526226
|
Unclassified |
Sporadic cancers |
|
rs199578185
|
Disease |
GM2-gangliosidosis 1 (GM2G1) [MIM:272800] |
|
rs387906885
|
Disease |
Mental retardation, autosomal recessive 15 (MRT15) [MIM:614202] |
|
rs387906886
|
Disease |
Mental retardation, autosomal recessive 15 (MRT15) [MIM:614202] |
|
rs748190164
|
Unclassified |
GM2-gangliosidosis 1 (GM2G1) [MIM:272800] |
|
hsa00520
|
Amino sugar and nucleotide sugar metabolism
|
|
dbSNP |
Type |
Disease name |
|
-
|
Disease |
Maturity-onset diabetes of the young 2 (MODY2) [MIM:125851] |
|
-
|
Disease |
Galactosemia II (GALCT2) [MIM:230200] |
|
-
|
Disease |
GM2-gangliosidosis 1 (GM2G1) [MIM:272800] |
|
-
|
Disease |
Nonaka myopathy (NM) [MIM:605820] |
|
-
|
Disease |
Diabetes mellitus, permanent neonatal (PNDM) [MIM:606176] |
|
-
|
Disease |
Congenital disorder of glycosylation 1T (CDG1T) [MIM:614921] |
|
rs104894009
|
Disease |
Maturity-onset diabetes of the young 2 (MODY2) [MIM:125851] |
|
rs1054374
|
Polymorphism |
- |
|
rs111033648
|
Disease |
Galactosemia (GALCT) [MIM:230400] |
|
rs111033652
|
Disease |
Galactosemia (GALCT) [MIM:230400] |
|
rs111033669
|
Disease |
Galactosemia (GALCT) [MIM:230400] |
|
rs111033715
|
Disease |
Galactosemia (GALCT) [MIM:230400] |
|
rs111033720
|
Disease |
Galactosemia (GALCT) [MIM:230400] |
|
rs111033802
|
Disease |
Galactosemia (GALCT) [MIM:230400] |
|
rs111033808
|
Disease |
Galactosemia (GALCT) [MIM:230400] |
|
rs111033809
|
Disease |
Galactosemia (GALCT) [MIM:230400] |
|
rs111033810
|
Disease |
Galactosemia (GALCT) [MIM:230400] |
|
rs111033812
|
Disease |
Galactosemia (GALCT) [MIM:230400] |
|
rs111033814
|
Disease |
Galactosemia (GALCT) [MIM:230400] |
|
rs111033815
|
Disease |
Galactosemia (GALCT) [MIM:230400] |
|
rs111033832
|
Disease |
Galactosemia (GALCT) [MIM:230400] |
|
rs1131691007
|
Unclassified |
Sporadic cancers |
|
rs1131691416
|
Disease |
Maturity-onset diabetes of the young 2 (MODY2) [MIM:125851] |
|
rs121908047
|
Disease |
Epimerase-deficiency galactosemia (EDG) [MIM:230350] |
|
rs121908633
|
Disease |
Nonaka myopathy (NM) [MIM:605820] |
|
rs1286804191
|
Disease |
Diabetes mellitus, permanent neonatal (PNDM) [MIM:606176] |
|
rs1320810473
|
Disease |
Congenital disorder of glycosylation 1T (CDG1T) [MIM:614921] |
|
rs1375656631
|
Disease |
Maturity-onset diabetes of the young 2 (MODY2) [MIM:125851] |
|
rs137853860
|
Disease |
Epimerase-deficiency galactosemia (EDG) [MIM:230350] |
|
rs137853861
|
Disease |
Epimerase-deficiency galactosemia (EDG) [MIM:230350] |
|
rs1441649062
|
Disease |
Maturity-onset diabetes of the young 2 (MODY2) [MIM:125851] |
|
rs1455785164
|
Disease |
Nonaka myopathy (NM) [MIM:605820] |
|
rs148311934
|
Disease |
Maturity-onset diabetes of the young 2 (MODY2) [MIM:125851] |
|
rs1554335135
|
Disease |
Maturity-onset diabetes of the young 2 (MODY2) [MIM:125851] |
|
rs1554658910
|
Disease |
Nonaka myopathy (NM) [MIM:605820] |
|
rs1554664064
|
Disease |
Nonaka myopathy (NM) [MIM:605820] |
|
rs1555526226
|
Unclassified |
Sporadic cancers |
|
rs1555748926
|
Disease |
Galactosemia II (GALCT2) [MIM:230200] |
|
rs193922272
|
Disease |
Maturity-onset diabetes of the young 2 (MODY2) [MIM:125851] |
|
rs193922282
|
Disease |
Diabetes mellitus, permanent neonatal (PNDM) [MIM:606176] |
|
rs193922297
|
Disease |
Maturity-onset diabetes of the young 2 (MODY2) [MIM:125851] |
|
rs193922311
|
Disease |
Maturity-onset diabetes of the young 2 (MODY2) [MIM:125851] |
|
rs199578185
|
Disease |
GM2-gangliosidosis 1 (GM2G1) [MIM:272800] |
|
rs367543259
|
Disease |
Galactosemia (GALCT) [MIM:230400] |
|
rs375690568
|
Disease |
Galactosemia II (GALCT2) [MIM:230200] |
|
rs398122379
|
Disease |
Hexokinase deficiency (HK deficiency) [MIM:235700] |
|
rs748190164
|
Unclassified |
GM2-gangliosidosis 1 (GM2G1) [MIM:272800] |
|
rs75391579
|
Disease |
Galactosemia (GALCT) [MIM:230400] |
|
rs754967473
|
Disease |
Galactosemia II (GALCT2) [MIM:230200] |
|
rs758737171
|
Disease |
Familial hyperinsulinemic hypoglycemia 3 (HHF3) [MIM:602485] |
|
rs769268803
|
Disease |
Maturity-onset diabetes of the young 2 (MODY2) [MIM:125851] |
|
rs773416476
|
Polymorphism |
- |
|
rs779694939
|
Disease |
Nonaka myopathy (NM) [MIM:605820] |
|
rs80356655
|
Disease |
Maturity-onset diabetes of the young 2 (MODY2) [MIM:125851] |
|
rs80356655
|
Disease |
Diabetes mellitus, permanent neonatal (PNDM) [MIM:606176] |
|
rs886043979
|
Disease |
Nonaka myopathy (NM) [MIM:605820] |
|
rn00521
|
Streptomycin biosynthesis
|
|
dbSNP |
Type |
Disease name |
|
-
|
Disease |
Maturity-onset diabetes of the young 2 (MODY2) [MIM:125851] |
|
-
|
Disease |
Diabetes mellitus, permanent neonatal (PNDM) [MIM:606176] |
|
-
|
Disease |
Congenital disorder of glycosylation 1T (CDG1T) [MIM:614921] |
|
rs104894009
|
Disease |
Maturity-onset diabetes of the young 2 (MODY2) [MIM:125851] |
|
rs104894015
|
Disease |
Familial hyperinsulinemic hypoglycemia 3 (HHF3) [MIM:602485] |
|
rs1131691416
|
Disease |
Maturity-onset diabetes of the young 2 (MODY2) [MIM:125851] |
|
rs1286804191
|
Disease |
Diabetes mellitus, permanent neonatal (PNDM) [MIM:606176] |
|
rs1320810473
|
Disease |
Congenital disorder of glycosylation 1T (CDG1T) [MIM:614921] |
|
rs1375656631
|
Disease |
Maturity-onset diabetes of the young 2 (MODY2) [MIM:125851] |
|
rs1441649062
|
Disease |
Maturity-onset diabetes of the young 2 (MODY2) [MIM:125851] |
|
rs147065275
|
Disease |
Maturity-onset diabetes of the young 2 (MODY2) [MIM:125851] |
|
rs148311934
|
Disease |
Maturity-onset diabetes of the young 2 (MODY2) [MIM:125851] |
|
rs1554335135
|
Disease |
Maturity-onset diabetes of the young 2 (MODY2) [MIM:125851] |
|
rs193922272
|
Disease |
Maturity-onset diabetes of the young 2 (MODY2) [MIM:125851] |
|
rs193922282
|
Disease |
Diabetes mellitus, permanent neonatal (PNDM) [MIM:606176] |
|
rs193922297
|
Disease |
Maturity-onset diabetes of the young 2 (MODY2) [MIM:125851] |
|
rs193922311
|
Disease |
Maturity-onset diabetes of the young 2 (MODY2) [MIM:125851] |
|
rs398122379
|
Disease |
Hexokinase deficiency (HK deficiency) [MIM:235700] |
|
rs758737171
|
Disease |
Familial hyperinsulinemic hypoglycemia 3 (HHF3) [MIM:602485] |
|
rs769268803
|
Disease |
Maturity-onset diabetes of the young 2 (MODY2) [MIM:125851] |
|
rs80356655
|
Disease |
Maturity-onset diabetes of the young 2 (MODY2) [MIM:125851] |
|
rs80356655
|
Disease |
Diabetes mellitus, permanent neonatal (PNDM) [MIM:606176] |
|
hsa00524
|
Neomycin, kanamycin and gentamicin biosynthesis
|
|
dbSNP |
Type |
Disease name |
|
-
|
Disease |
Maturity-onset diabetes of the young 2 (MODY2) [MIM:125851] |
|
-
|
Disease |
Diabetes mellitus, permanent neonatal (PNDM) [MIM:606176] |
|
rs104894009
|
Disease |
Maturity-onset diabetes of the young 2 (MODY2) [MIM:125851] |
|
rs104894015
|
Disease |
Familial hyperinsulinemic hypoglycemia 3 (HHF3) [MIM:602485] |
|
rs1131691416
|
Disease |
Maturity-onset diabetes of the young 2 (MODY2) [MIM:125851] |
|
rs1286804191
|
Disease |
Diabetes mellitus, permanent neonatal (PNDM) [MIM:606176] |
|
rs1375656631
|
Disease |
Maturity-onset diabetes of the young 2 (MODY2) [MIM:125851] |
|
rs1441649062
|
Disease |
Maturity-onset diabetes of the young 2 (MODY2) [MIM:125851] |
|
rs147065275
|
Disease |
Maturity-onset diabetes of the young 2 (MODY2) [MIM:125851] |
|
rs148311934
|
Disease |
Maturity-onset diabetes of the young 2 (MODY2) [MIM:125851] |
|
rs1554335135
|
Disease |
Maturity-onset diabetes of the young 2 (MODY2) [MIM:125851] |
|
rs193922272
|
Disease |
Maturity-onset diabetes of the young 2 (MODY2) [MIM:125851] |
|
rs193922282
|
Disease |
Diabetes mellitus, permanent neonatal (PNDM) [MIM:606176] |
|
rs193922297
|
Disease |
Maturity-onset diabetes of the young 2 (MODY2) [MIM:125851] |
|
rs193922311
|
Disease |
Maturity-onset diabetes of the young 2 (MODY2) [MIM:125851] |
|
rs398122379
|
Disease |
Hexokinase deficiency (HK deficiency) [MIM:235700] |
|
rs758737171
|
Disease |
Familial hyperinsulinemic hypoglycemia 3 (HHF3) [MIM:602485] |
|
rs769268803
|
Disease |
Maturity-onset diabetes of the young 2 (MODY2) [MIM:125851] |
|
rs80356655
|
Disease |
Maturity-onset diabetes of the young 2 (MODY2) [MIM:125851] |
|
rs80356655
|
Disease |
Diabetes mellitus, permanent neonatal (PNDM) [MIM:606176] |
|
hsa00531
|
Glycosaminoglycan degradation
|
|
dbSNP |
Type |
Disease name |
|
-
|
Disease |
GM1-gangliosidosis 1 (GM1G1) [MIM:230500] |
|
-
|
Disease |
GM1-gangliosidosis 2 (GM1G2) [MIM:230600] |
|
-
|
Disease |
Mucopolysaccharidosis 3B (MPS3B) [MIM:252920] |
|
-
|
Disease |
GM2-gangliosidosis 1 (GM2G1) [MIM:272800] |
|
-
|
Disease |
Mucopolysaccharidosis 1H (MPS1H) [MIM:607014] |
|
-
|
Disease |
Mucopolysaccharidosis 1S (MPS1S) [MIM:607016] |
|
rs1054374
|
Polymorphism |
- |
|
rs1131691007
|
Unclassified |
Sporadic cancers |
|
rs1553612220
|
Disease |
Mucopolysaccharidosis 4B (MPS4B) [MIM:253010] |
|
rs1555526226
|
Unclassified |
Sporadic cancers |
|
rs199578185
|
Disease |
GM2-gangliosidosis 1 (GM2G1) [MIM:272800] |
|
rs376663785
|
Disease |
GM1-gangliosidosis 3 (GM1G3) [MIM:230650] |
|
rs558683362
|
Disease |
Mucopolysaccharidosis 1H (MPS1H) [MIM:607014] |
|
rs72555362
|
Disease |
Mucopolysaccharidosis 4B (MPS4B) [MIM:253010] |
|
rs748190164
|
Unclassified |
GM2-gangliosidosis 1 (GM2G1) [MIM:272800] |
|
rs750496798
|
Disease |
Mucopolysaccharidosis 1H/S (MPS1H/S) [MIM:607015] |
|
rs754154200
|
Disease |
Mucopolysaccharidosis 1H (MPS1H) [MIM:607014] |
|
rs754966840
|
Disease |
Mucopolysaccharidosis 1S (MPS1S) [MIM:607016] |
|
rs794726877
|
Disease |
Mucopolysaccharidosis 1H (MPS1H) [MIM:607014] |
|
rs879050821
|
Disease |
GM1-gangliosidosis 1 (GM1G1) [MIM:230500] |
|
rs886042079
|
Polymorphism |
- |
|
rs968221254
|
Disease |
Mucopolysaccharidosis 4B (MPS4B) [MIM:253010] |
|
hsa00561
|
Glycerolipid metabolism
|
|
dbSNP |
Type |
Disease name |
|
-
|
Disease |
Fabry disease (FD) [MIM:301500] |
|
rs104894840
|
Disease |
Fabry disease (FD) [MIM:301500] |
|
rs104894845
|
Unclassified |
Fabry disease (FD) [MIM:301500] |
|
rs113173389
|
Disease |
Fabry disease (FD) [MIM:301500] |
|
rs121912707
|
Disease |
Pyridoxine-dependent epilepsy (PDE) [MIM:266100] |
|
rs121912711
|
Disease |
Pyridoxine-dependent epilepsy (PDE) [MIM:266100] |
|
rs5054
|
Polymorphism |
- |
|
rs5056
|
Polymorphism |
- |
|
rs727505292
|
Unclassified |
Fabry disease (FD) [MIM:301500] |
|
rs730880451
|
Disease |
Fabry disease (FD) [MIM:301500] |
|
rs869312153
|
Unclassified |
Fabry disease (FD) [MIM:301500] |
|
rs869312160
|
Disease |
Fabry disease (FD) [MIM:301500] |
|
rs869312161
|
Unclassified |
Fabry disease (FD) [MIM:301500] |
|
rs869312214
|
Disease |
Fabry disease (FD) [MIM:301500] |
|
rs869312254
|
Disease |
Fabry disease (FD) [MIM:301500] |
|
rs869312256
|
Disease |
Fabry disease (FD) [MIM:301500] |
|
rs869312270
|
Disease |
Fabry disease (FD) [MIM:301500] |
|
rs869312393
|
Disease |
Fabry disease (FD) [MIM:301500] |
|
rs886041315
|
Disease |
Fabry disease (FD) [MIM:301500] |
|
rs886044845
|
Disease |
Fabry disease (FD) [MIM:301500] |
|
hsa00562
|
Inositol phosphate metabolism
|
|
dbSNP |
Type |
Disease name |
|
-
|
Disease |
Epileptic encephalopathy, infantile or early childhood, 1 (IECEE1) [MIM:617711] |
|
rs137853842
|
Disease |
Lowe oculocerebrorenal syndrome (OCRL) [MIM:309000] |
|
rs137853846
|
Disease |
Dent disease 2 (DD2) [MIM:300555] |
|
rs137853848
|
Disease |
Lowe oculocerebrorenal syndrome (OCRL) [MIM:309000] |
|
rs137853852
|
Disease |
Lowe oculocerebrorenal syndrome (OCRL) [MIM:309000] |
|
rs137853853
|
Disease |
Lowe oculocerebrorenal syndrome (OCRL) [MIM:309000] |
|
rs137853856
|
Disease |
Lowe oculocerebrorenal syndrome (OCRL) [MIM:309000] |
|
rs137853857
|
Disease |
Lowe oculocerebrorenal syndrome (OCRL) [MIM:309000] |
|
rs1553923787
|
Disease |
Epileptic encephalopathy, infantile or early childhood, 1 (IECEE1) [MIM:617711] |
|
rs1553925558
|
Disease |
Epileptic encephalopathy, infantile or early childhood, 1 (IECEE1) [MIM:617711] |
|
rs863225460
|
Disease |
Megalencephaly-capillary malformation-polymicrogyria syndrome (MCAP) [MIM:602501] |
|
hsa00564
|
Glycerophospholipid metabolism
|
|
dbSNP |
Type |
Disease name |
|
-
|
Disease |
Butyrylcholinesterase deficiency (BCHED) [MIM:617936] |
|
rs121912819
|
Disease |
Myasthenic syndrome, congenital, 6, presynaptic (CMS6) [MIM:254210] |
|
rs121918558
|
Disease |
Butyrylcholinesterase deficiency (BCHED) [MIM:617936] |
|
rs201820739
|
Disease |
Butyrylcholinesterase deficiency (BCHED) [MIM:617936] |
|
rs2232202
|
Polymorphism |
- |
|
rs370077923
|
Disease |
Butyrylcholinesterase deficiency (BCHED) [MIM:617936] |
|
rs531738678
|
Disease |
Butyrylcholinesterase deficiency (BCHED) [MIM:617936] |
|
rs747598704
|
Disease |
Butyrylcholinesterase deficiency (BCHED) [MIM:617936] |
|
rs770337031
|
Disease |
Butyrylcholinesterase deficiency (BCHED) [MIM:617936] |
|
hsa00565
|
Ether lipid metabolism
|
|
dbSNP |
Type |
Disease name |
|
rs1051931
|
Polymorphism |
- |
|
rs45454695
|
Polymorphism |
- |
|
hsa00590
|
Arachidonic acid metabolism
|
|
dbSNP |
Type |
Disease name |
|
-
|
Disease |
46,XY sex reversal 8 (SRXY8) [MIM:614279] |
|
rs1056892
|
Polymorphism |
- |
|
rs121434480
|
Disease |
Cranioosteoarthropathy (COA) [MIM:259100] |
|
rs121434481
|
Disease |
Isolated congenital nail clubbing (ICNC) [MIM:119900] |
|
rs138142612
|
Polymorphism |
- |
|
rs17004876
|
Polymorphism |
- |
|
rs17884712
|
Polymorphism |
- |
|
rs188934928
|
Polymorphism |
- |
|
rs192154563
|
Polymorphism |
- |
|
rs2835285
|
Polymorphism |
- |
|
rs28399505
|
Polymorphism |
- |
|
rs3758581
|
Polymorphism |
- |
|
rs41291556
|
Polymorphism |
- |
|
rs56337013
|
Polymorphism |
- |
|
rs7225107
|
Polymorphism |
- |
|
rs72552267
|
Polymorphism |
- |
|
rs797044460
|
Disease |
46,XY sex reversal 8 (SRXY8) [MIM:614279] |
|
rs8177445
|
Polymorphism |
- |
|
hsa00591
|
Linoleic acid metabolism
|
|
dbSNP |
Type |
Disease name |
|
-
|
Disease |
Glaucoma 3, primary congenital, A (GLC3A) [MIM:231300] |
|
rs1041988
|
Polymorphism |
- |
|
rs104893628
|
Disease |
Glaucoma 3, primary congenital, A (GLC3A) [MIM:231300] |
|
rs12721627
|
Polymorphism |
- |
|
rs12721629
|
Polymorphism |
- |
|
rs138142612
|
Polymorphism |
- |
|
rs17884712
|
Polymorphism |
- |
|
rs188934928
|
Polymorphism |
- |
|
rs192154563
|
Polymorphism |
- |
|
rs28371759
|
Polymorphism |
- |
|
rs28936701
|
Disease |
Glaucoma 3, primary congenital, A (GLC3A) [MIM:231300] |
|
rs3208363
|
Polymorphism |
- |
|
rs3758581
|
Polymorphism |
- |
|
rs41291556
|
Polymorphism |
- |
|
rs4986908
|
Polymorphism |
- |
|
rs4986910
|
Polymorphism |
- |
|
rs4987161
|
Polymorphism |
- |
|
rs55785340
|
Polymorphism |
- |
|
rs55951658
|
Polymorphism |
- |
|
rs56324128
|
Polymorphism |
- |
|
rs56337013
|
Polymorphism |
- |
|
rs57865060
|
Disease |
Glaucoma 3, primary congenital, A (GLC3A) [MIM:231300] |
|
rs67784355
|
Polymorphism |
- |
|
rs7225107
|
Polymorphism |
- |
|
rs72549378
|
Disease |
Glaucoma 3, primary congenital, A (GLC3A) [MIM:231300] |
|
rs72552267
|
Polymorphism |
- |
|
rs72552799
|
Polymorphism |
- |
|
rs752456881
|
Polymorphism |
- |
|
rs9282670
|
Polymorphism |
- |
|
rs9341250
|
Polymorphism |
- |
|
hsa00592
|
alpha-Linolenic acid metabolism
|
|
dbSNP |
Type |
Disease name |
|
rs1041969
|
Polymorphism |
- |
|
rs104886492
|
Unclassified |
HDS10 mitochondrial disease (HSD10MD) [MIM:300438] |
|
rs1229984
|
Polymorphism |
- |
|
rs137853096
|
Disease |
D-bifunctional protein deficiency (DBPD) [MIM:261515] |
|
rs137853101
|
Disease |
3-alpha-hydroxyacyl-CoA dehydrogenase deficiency (HADH deficiency) [MIM:231530] |
|
rs137853102
|
Disease |
3-alpha-hydroxyacyl-CoA dehydrogenase deficiency (HADH deficiency) [MIM:231530] |
|
rs2066702
|
Polymorphism |
- |
|
rs28730628
|
Polymorphism |
- |
|
rs35385902
|
Polymorphism |
- |
|
hsa00600
|
Sphingolipid metabolism
|
|
dbSNP |
Type |
Disease name |
|
-
|
Disease |
GM1-gangliosidosis 1 (GM1G1) [MIM:230500] |
|
-
|
Disease |
GM1-gangliosidosis 2 (GM1G2) [MIM:230600] |
|
-
|
Disease |
Gaucher disease 1 (GD1) [MIM:230800] |
|
-
|
Disease |
Gaucher disease 2 (GD2) [MIM:230900] |
|
-
|
Disease |
Fabry disease (FD) [MIM:301500] |
|
rs104894840
|
Disease |
Fabry disease (FD) [MIM:301500] |
|
rs104894845
|
Unclassified |
Fabry disease (FD) [MIM:301500] |
|
rs113173389
|
Disease |
Fabry disease (FD) [MIM:301500] |
|
rs1141811
|
Disease |
Gaucher disease (GD) [MIM:230800] |
|
rs1553612220
|
Disease |
Mucopolysaccharidosis 4B (MPS4B) [MIM:253010] |
|
rs376663785
|
Disease |
GM1-gangliosidosis 3 (GM1G3) [MIM:230650] |
|
rs72555362
|
Disease |
Mucopolysaccharidosis 4B (MPS4B) [MIM:253010] |
|
rs727505292
|
Unclassified |
Fabry disease (FD) [MIM:301500] |
|
rs730880451
|
Disease |
Fabry disease (FD) [MIM:301500] |
|
rs77369218
|
Disease |
Gaucher disease (GD) [MIM:230800] |
|
rs77829017
|
Disease |
Gaucher disease (GD) [MIM:230800] |
|
rs869312153
|
Unclassified |
Fabry disease (FD) [MIM:301500] |
|
rs869312160
|
Disease |
Fabry disease (FD) [MIM:301500] |
|
rs869312161
|
Unclassified |
Fabry disease (FD) [MIM:301500] |
|
rs869312214
|
Disease |
Fabry disease (FD) [MIM:301500] |
|
rs869312254
|
Disease |
Fabry disease (FD) [MIM:301500] |
|
rs869312256
|
Disease |
Fabry disease (FD) [MIM:301500] |
|
rs869312270
|
Disease |
Fabry disease (FD) [MIM:301500] |
|
rs869312393
|
Disease |
Fabry disease (FD) [MIM:301500] |
|
rs879050821
|
Disease |
GM1-gangliosidosis 1 (GM1G1) [MIM:230500] |
|
rs886041315
|
Disease |
Fabry disease (FD) [MIM:301500] |
|
rs886042079
|
Polymorphism |
- |
|
rs886044845
|
Disease |
Fabry disease (FD) [MIM:301500] |
|
rs968221254
|
Disease |
Mucopolysaccharidosis 4B (MPS4B) [MIM:253010] |
|
hsa00603
|
Glycosphingolipid biosynthesis - globo and isoglobo series
|
|
dbSNP |
Type |
Disease name |
|
-
|
Disease |
Fabry disease (FD) [MIM:301500] |
|
rs104894840
|
Disease |
Fabry disease (FD) [MIM:301500] |
|
rs104894845
|
Unclassified |
Fabry disease (FD) [MIM:301500] |
|
rs113173389
|
Disease |
Fabry disease (FD) [MIM:301500] |
|
rs727505292
|
Unclassified |
Fabry disease (FD) [MIM:301500] |
|
rs730880451
|
Disease |
Fabry disease (FD) [MIM:301500] |
|
rs869312153
|
Unclassified |
Fabry disease (FD) [MIM:301500] |
|
rs869312160
|
Disease |
Fabry disease (FD) [MIM:301500] |
|
rs869312161
|
Unclassified |
Fabry disease (FD) [MIM:301500] |
|
rs869312214
|
Disease |
Fabry disease (FD) [MIM:301500] |
|
rs869312254
|
Disease |
Fabry disease (FD) [MIM:301500] |
|
rs869312256
|
Disease |
Fabry disease (FD) [MIM:301500] |
|
rs869312270
|
Disease |
Fabry disease (FD) [MIM:301500] |
|
rs869312393
|
Disease |
Fabry disease (FD) [MIM:301500] |
|
rs886041315
|
Disease |
Fabry disease (FD) [MIM:301500] |
|
rs886044845
|
Disease |
Fabry disease (FD) [MIM:301500] |
|
hsa00604
|
Glycosphingolipid biosynthesis - ganglio series
|
|
dbSNP |
Type |
Disease name |
|
-
|
Disease |
GM1-gangliosidosis 1 (GM1G1) [MIM:230500] |
|
-
|
Disease |
GM1-gangliosidosis 2 (GM1G2) [MIM:230600] |
|
rs1553612220
|
Disease |
Mucopolysaccharidosis 4B (MPS4B) [MIM:253010] |
|
rs376663785
|
Disease |
GM1-gangliosidosis 3 (GM1G3) [MIM:230650] |
|
rs72555362
|
Disease |
Mucopolysaccharidosis 4B (MPS4B) [MIM:253010] |
|
rs879050821
|
Disease |
GM1-gangliosidosis 1 (GM1G1) [MIM:230500] |
|
rs886042079
|
Polymorphism |
- |
|
rs968221254
|
Disease |
Mucopolysaccharidosis 4B (MPS4B) [MIM:253010] |
|
hsa00620
|
Pyruvate metabolism
|
|
dbSNP |
Type |
Disease name |
|
-
|
Disease |
Pyruvate kinase deficiency of red cells (PKRD) [MIM:266200] |
|
-
|
Disease |
Pyruvate dehydrogenase E1-alpha deficiency (PDHAD) [MIM:312170] |
|
-
|
Disease |
Microphthalmia, isolated, 8 (MCOP8) [MIM:615113] |
|
rs1041969
|
Polymorphism |
- |
|
rs1167329263
|
Disease |
Pyruvate kinase deficiency of red cells (PKRD) [MIM:266200] |
|
rs120074141
|
Disease |
3-ketothiolase deficiency (3KTD) [MIM:203750] |
|
rs121912707
|
Disease |
Pyridoxine-dependent epilepsy (PDE) [MIM:266100] |
|
rs121912711
|
Disease |
Pyridoxine-dependent epilepsy (PDE) [MIM:266100] |
|
rs121964988
|
Disease |
Dihydrolipoamide dehydrogenase deficiency (DLDD) [MIM:246900] |
|
rs121964991
|
Disease |
Dihydrolipoamide dehydrogenase deficiency (DLDD) [MIM:246900] |
|
rs121964993
|
Disease |
Dihydrolipoamide dehydrogenase deficiency (DLDD) [MIM:246900] |
|
rs1229984
|
Polymorphism |
- |
|
rs1357271377
|
Unclassified |
A colorectal cancer sample |
|
rs137853258
|
Disease |
Pyruvate dehydrogenase E1-alpha deficiency (PDHAD) [MIM:312170] |
|
rs16952692
|
Polymorphism |
- |
|
rs17853396
|
Polymorphism |
- |
|
rs17855424
|
Polymorphism |
- |
|
rs2066702
|
Polymorphism |
- |
|
rs28359542
|
Polymorphism |
- |
|
rs28383586
|
Polymorphism |
- |
|
rs28730628
|
Polymorphism |
- |
|
rs28940589
|
Disease |
Pyruvate carboxylase deficiency (PC deficiency) [MIM:266150] |
|
rs28940590
|
Disease |
Pyruvate carboxylase deficiency (PC deficiency) [MIM:266150] |
|
rs35385902
|
Polymorphism |
- |
|
rs671
|
Polymorphism |
- |
|
rs747097960
|
Disease |
Pyruvate kinase deficiency of red cells (PKRD) [MIM:266200] |
|
rs769724893
|
Polymorphism |
- |
|
rs777954556
|
Disease |
Lactate dehydrogenase B deficiency (LDHBD) [MIM:614128] |
|
rs782308462
|
Disease |
Epileptic encephalopathy, early infantile, 51 (EIEE51) [MIM:617339] |
|
rs981505482
|
Disease |
Pyruvate kinase deficiency of red cells (PKRD) [MIM:266200] |
|
rn00621
|
Dioxin degradation
|
|
dbSNP |
Type |
Disease name |
|
rs1041969
|
Polymorphism |
- |
|
rs1229984
|
Polymorphism |
- |
|
rs2066702
|
Polymorphism |
- |
|
rs28730628
|
Polymorphism |
- |
|
rs35385902
|
Polymorphism |
- |
|
rn00622
|
Xylene degradation
|
|
dbSNP |
Type |
Disease name |
|
rs1041969
|
Polymorphism |
- |
|
rs1229984
|
Polymorphism |
- |
|
rs2066702
|
Polymorphism |
- |
|
rs28730628
|
Polymorphism |
- |
|
rs35385902
|
Polymorphism |
- |
|
rn00623
|
Toluene degradation
|
|
dbSNP |
Type |
Disease name |
|
rs104886492
|
Unclassified |
HDS10 mitochondrial disease (HSD10MD) [MIM:300438] |
|
rs137853096
|
Disease |
D-bifunctional protein deficiency (DBPD) [MIM:261515] |
|
rs137853101
|
Disease |
3-alpha-hydroxyacyl-CoA dehydrogenase deficiency (HADH deficiency) [MIM:231530] |
|
rs137853102
|
Disease |
3-alpha-hydroxyacyl-CoA dehydrogenase deficiency (HADH deficiency) [MIM:231530] |
|
rn00625
|
Chloroalkane and chloroalkene degradation
|
|
dbSNP |
Type |
Disease name |
|
rs1041969
|
Polymorphism |
- |
|
rs121912707
|
Disease |
Pyridoxine-dependent epilepsy (PDE) [MIM:266100] |
|
rs121912711
|
Disease |
Pyridoxine-dependent epilepsy (PDE) [MIM:266100] |
|
rs1229984
|
Polymorphism |
- |
|
rs2066702
|
Polymorphism |
- |
|
rs28730628
|
Polymorphism |
- |
|
rs35385902
|
Polymorphism |
- |
|
rs751141
|
Polymorphism |
- |
|
rn00626
|
Naphthalene degradation
|
|
dbSNP |
Type |
Disease name |
|
rs1041969
|
Polymorphism |
- |
|
rs1229984
|
Polymorphism |
- |
|
rs2066702
|
Polymorphism |
- |
|
rs28730628
|
Polymorphism |
- |
|
rs35385902
|
Polymorphism |
- |
|
rn00627
|
Aminobenzoate degradation
|
|
dbSNP |
Type |
Disease name |
|
rs1048988
|
Polymorphism |
- |
|
rs1048994
|
Polymorphism |
- |
|
hsa00630
|
Glyoxylate and dicarboxylate metabolism
|
|
dbSNP |
Type |
Disease name |
|
-
|
Disease |
Canavan disease (CAND) [MIM:271900] |
|
rs1014551540
|
Disease |
Canavan disease (CAND) [MIM:271900] |
|
rs104894550
|
Disease |
Canavan disease (CAND) [MIM:271900] |
|
rs115014558
|
Polymorphism |
- |
|
rs120074141
|
Disease |
3-ketothiolase deficiency (3KTD) [MIM:203750] |
|
rs121908520
|
Disease |
Hyperoxaluria primary 1 (HP1) [MIM:259900] |
|
rs121908524
|
Disease |
Hyperoxaluria primary 1 (HP1) [MIM:259900] |
|
rs121908527
|
Disease |
Hyperoxaluria primary 1 (HP1) [MIM:259900] |
|
rs121908530
|
Disease |
Hyperoxaluria primary 1 (HP1) [MIM:259900] |
|
rs121964988
|
Disease |
Dihydrolipoamide dehydrogenase deficiency (DLDD) [MIM:246900] |
|
rs121964991
|
Disease |
Dihydrolipoamide dehydrogenase deficiency (DLDD) [MIM:246900] |
|
rs121964993
|
Disease |
Dihydrolipoamide dehydrogenase deficiency (DLDD) [MIM:246900] |
|
rs13408961
|
Polymorphism |
- |
|
rs1357271377
|
Unclassified |
A colorectal cancer sample |
|
rs138207257
|
Disease |
Hyperoxaluria primary 3 (HP3) [MIM:613616] |
|
rs140992177
|
Polymorphism |
- |
|
rs1414684396
|
Disease |
Canavan disease (CAND) [MIM:271900] |
|
rs1555538144
|
Disease |
Canavan disease (CAND) [MIM:271900] |
|
rs1555538148
|
Disease |
Canavan disease (CAND) [MIM:271900] |
|
rs1555538151
|
Disease |
Canavan disease (CAND) [MIM:271900] |
|
rs180177155
|
Disease |
Hyperoxaluria primary 1 (HP1) [MIM:259900] |
|
rs180177156
|
Disease |
Hyperoxaluria primary 1 (HP1) [MIM:259900] |
|
rs180177157
|
Disease |
Hyperoxaluria primary 1 (HP1) [MIM:259900] |
|
rs180177173
|
Disease |
Hyperoxaluria primary 1 (HP1) [MIM:259900] |
|
rs180177185
|
Disease |
Hyperoxaluria primary 1 (HP1) [MIM:259900] |
|
rs180177197
|
Disease |
Hyperoxaluria primary 1 (HP1) [MIM:259900] |
|
rs180177225
|
Disease |
Hyperoxaluria primary 1 (HP1) [MIM:259900] |
|
rs180177236
|
Disease |
Hyperoxaluria primary 1 (HP1) [MIM:259900] |
|
rs180177244
|
Disease |
Hyperoxaluria primary 1 (HP1) [MIM:259900] |
|
rs180177253
|
Disease |
Hyperoxaluria primary 1 (HP1) [MIM:259900] |
|
rs180177264
|
Disease |
Hyperoxaluria primary 1 (HP1) [MIM:259900] |
|
rs180177289
|
Disease |
Hyperoxaluria primary 1 (HP1) [MIM:259900] |
|
rs180177290
|
Disease |
Hyperoxaluria primary 1 (HP1) [MIM:259900] |
|
rs28940279
|
Disease |
Canavan disease (CAND) [MIM:271900] |
|
rs34885252
|
Polymorphism |
- |
|
rs4426527
|
Polymorphism |
- |
|
rs73106685
|
Polymorphism |
- |
|
rs773049803
|
Disease |
Canavan disease (CAND) [MIM:271900] |
|
rs774323189
|
Disease |
Canavan disease (CAND) [MIM:271900] |
|
rs776777887
|
Disease |
Canavan disease (CAND) [MIM:271900] |
|
rs777936704
|
Disease |
Canavan disease (CAND) [MIM:271900] |
|
rs782308462
|
Disease |
Epileptic encephalopathy, early infantile, 51 (EIEE51) [MIM:617339] |
|
rs796052061
|
Disease |
Hyperoxaluria primary 1 (HP1) [MIM:259900] |
|
rs80358214
|
Disease |
Congenital systemic glutamine deficiency (CSGD) [MIM:610015] |
|
rs937670540
|
Disease |
Canavan disease (CAND) [MIM:271900] |
|
rn00633
|
Nitrotoluene degradation
|
|
dbSNP |
Type |
Disease name |
|
rs1799931
|
Polymorphism |
- |
|
rs4986996
|
Polymorphism |
- |
|
rs56387565
|
Polymorphism |
- |
|
hsa00640
|
Propanoate metabolism
|
|
dbSNP |
Type |
Disease name |
|
rs120074141
|
Disease |
3-ketothiolase deficiency (3KTD) [MIM:203750] |
|
rs121918329
|
Disease |
3-hydroxyisobutryl-CoA hydrolase deficiency (HIBCHD) [MIM:250620] |
|
rs121964988
|
Disease |
Dihydrolipoamide dehydrogenase deficiency (DLDD) [MIM:246900] |
|
rs121964991
|
Disease |
Dihydrolipoamide dehydrogenase deficiency (DLDD) [MIM:246900] |
|
rs121964993
|
Disease |
Dihydrolipoamide dehydrogenase deficiency (DLDD) [MIM:246900] |
|
rs1357271377
|
Unclassified |
A colorectal cancer sample |
|
rs777954556
|
Disease |
Lactate dehydrogenase B deficiency (LDHBD) [MIM:614128] |
|
rn00643
|
Styrene degradation
|
|
dbSNP |
Type |
Disease name |
|
-
|
Disease |
Microphthalmia, isolated, 8 (MCOP8) [MIM:615113] |
|
hsa00650
|
Butanoate metabolism
|
|
dbSNP |
Type |
Disease name |
|
-
|
Disease |
Succinyl-CoA:3-oxoacid CoA transferase deficiency (SCOTD) [MIM:245050] |
|
-
|
Disease |
3-hydroxy-3-methylglutaryl-CoA lyase deficiency (HMGCLD) [MIM:246450] |
|
-
|
Disease |
Succinic semialdehyde dehydrogenase deficiency (SSADHD) [MIM:271980] |
|
rs1041969
|
Polymorphism |
- |
|
rs104886492
|
Unclassified |
HDS10 mitochondrial disease (HSD10MD) [MIM:300438] |
|
rs120074141
|
Disease |
3-ketothiolase deficiency (3KTD) [MIM:203750] |
|
rs121434275
|
Disease |
Acyl-CoA dehydrogenase medium-chain deficiency (ACADMD) [MIM:201450] |
|
rs121434278
|
Disease |
Acyl-CoA dehydrogenase medium-chain deficiency (ACADMD) [MIM:201450] |
|
rs121434279
|
Disease |
Acyl-CoA dehydrogenase medium-chain deficiency (ACADMD) [MIM:201450] |
|
rs121434281
|
Disease |
Acyl-CoA dehydrogenase medium-chain deficiency (ACADMD) [MIM:201450] |
|
rs121434283
|
Disease |
Acyl-CoA dehydrogenase medium-chain deficiency (ACADMD) [MIM:201450] |
|
rs121909301
|
Disease |
Succinyl-CoA:3-oxoacid CoA transferase deficiency (SCOTD) [MIM:245050] |
|
rs1229984
|
Polymorphism |
- |
|
rs1326526453
|
Disease |
Succinic semialdehyde dehydrogenase deficiency (SSADHD) [MIM:271980] |
|
rs1327401976
|
Disease |
Succinyl-CoA:3-oxoacid CoA transferase deficiency (SCOTD) [MIM:245050] |
|
rs1357942068
|
Disease |
3-hydroxy-3-methylglutaryl-CoA lyase deficiency (HMGCLD) [MIM:246450] |
|
rs137852640
|
Disease |
3-hydroxy-3-methylglutaryl-CoA synthase-2 deficiency (HMGCS2D) [MIM:605911] |
|
rs137853096
|
Disease |
D-bifunctional protein deficiency (DBPD) [MIM:261515] |
|
rs137853101
|
Disease |
3-alpha-hydroxyacyl-CoA dehydrogenase deficiency (HADH deficiency) [MIM:231530] |
|
rs137853102
|
Disease |
3-alpha-hydroxyacyl-CoA dehydrogenase deficiency (HADH deficiency) [MIM:231530] |
|
rs145087265
|
Disease |
Succinic semialdehyde dehydrogenase deficiency (SSADHD) [MIM:271980] |
|
rs1553131940
|
Disease |
3-hydroxy-3-methylglutaryl-CoA lyase deficiency (HMGCLD) [MIM:246450] |
|
rs199587895
|
Disease |
3-hydroxy-3-methylglutaryl-CoA lyase deficiency (HMGCLD) [MIM:246450] |
|
rs2066702
|
Polymorphism |
- |
|
rs28730628
|
Polymorphism |
- |
|
rs35385902
|
Polymorphism |
- |
|
rs375628463
|
Disease |
Succinic semialdehyde dehydrogenase deficiency (SSADHD) [MIM:271980] |
|
rs4586421
|
Polymorphism |
- |
|
rs62621664
|
Polymorphism |
- |
|
rs72552283
|
Disease |
Succinic semialdehyde dehydrogenase deficiency (SSADHD) [MIM:271980] |
|
rs727503963
|
Disease |
3-hydroxy-3-methylglutaryl-CoA lyase deficiency (HMGCLD) [MIM:246450] |
|
rs760106433
|
Disease |
3-hydroxy-3-methylglutaryl-CoA lyase deficiency (HMGCLD) [MIM:246450] |
|
rs765561257
|
Disease |
Succinic semialdehyde dehydrogenase deficiency (SSADHD) [MIM:271980] |
|
hsa00670
|
One carbon pool by folate
|
|
dbSNP |
Type |
Disease name |
|
-
|
Disease |
Methylenetetrahydrofolate reductase deficiency (MTHFRD) [MIM:236250] |
|
-
|
Disease |
Neurodevelopmental disorder with microcephaly, epilepsy, and hypomyelination (NEDMEHM) [MIM:618367] |
|
rs1182635980
|
Disease |
Methylenetetrahydrofolate reductase deficiency (MTHFRD) [MIM:236250] |
|
rs121434295
|
Disease |
Methylenetetrahydrofolate reductase deficiency (MTHFRD) [MIM:236250] |
|
rs121434297
|
Disease |
Methylenetetrahydrofolate reductase deficiency (MTHFRD) [MIM:236250] |
|
rs141210410
|
Disease |
Combined immunodeficiency and megaloblastic anemia with or without hyperhomocysteinemia (CIMAH) [MIM:617780] |
|
rs144508139
|
Disease |
Methylenetetrahydrofolate reductase deficiency (MTHFRD) [MIM:236250] |
|
rs1555336810
|
Disease |
Combined immunodeficiency and megaloblastic anemia with or without hyperhomocysteinemia (CIMAH) [MIM:617780] |
|
rs1555337681
|
Disease |
Combined immunodeficiency and megaloblastic anemia with or without hyperhomocysteinemia (CIMAH) [MIM:617780] |
|
rs1950902
|
Polymorphism |
- |
|
rs200100285
|
Disease |
Methylenetetrahydrofolate reductase deficiency (MTHFRD) [MIM:236250] |
|
rs201618781
|
Disease |
Methylenetetrahydrofolate reductase deficiency (MTHFRD) [MIM:236250] |
|
rs267606887
|
Disease |
Methylenetetrahydrofolate reductase deficiency (MTHFRD) [MIM:236250] |
|
rs34181110
|
Disease |
Neural tube defects, folate-sensitive (NTDFS) [MIM:601634] |
|
rs370444838
|
Disease |
Combined immunodeficiency and megaloblastic anemia with or without hyperhomocysteinemia (CIMAH) [MIM:617780] |
|
rs371085894
|
Disease |
Methylenetetrahydrofolate reductase deficiency (MTHFRD) [MIM:236250] |
|
rs373398993
|
Disease |
Methylenetetrahydrofolate reductase deficiency (MTHFRD) [MIM:236250] |
|
rs387906619
|
Disease |
Megaloblastic anemia due to dihydrofolate reductase deficiency (DHFRD) [MIM:613839] |
|
rs748571395
|
Disease |
Methylenetetrahydrofolate reductase deficiency (MTHFRD) [MIM:236250] |
|
rs754015864
|
Disease |
Methylenetetrahydrofolate reductase deficiency (MTHFRD) [MIM:236250] |
|
rs754980119
|
Disease |
Methylenetetrahydrofolate reductase deficiency (MTHFRD) [MIM:236250] |
|
rs760161369
|
Disease |
Methylenetetrahydrofolate reductase deficiency (MTHFRD) [MIM:236250] |
|
rs767890671
|
Disease |
Methylenetetrahydrofolate reductase deficiency (MTHFRD) [MIM:236250] |
|
rs769381688
|
Disease |
Methylenetetrahydrofolate reductase deficiency (MTHFRD) [MIM:236250] |
|
rs786204009
|
Disease |
Methylenetetrahydrofolate reductase deficiency (MTHFRD) [MIM:236250] |
|
rs786204014
|
Disease |
Methylenetetrahydrofolate reductase deficiency (MTHFRD) [MIM:236250] |
|
rs786204017
|
Disease |
Methylenetetrahydrofolate reductase deficiency (MTHFRD) [MIM:236250] |
|
rs786204018
|
Disease |
Methylenetetrahydrofolate reductase deficiency (MTHFRD) [MIM:236250] |
|
rs786204019
|
Disease |
Methylenetetrahydrofolate reductase deficiency (MTHFRD) [MIM:236250] |
|
rs786204021
|
Disease |
Methylenetetrahydrofolate reductase deficiency (MTHFRD) [MIM:236250] |
|
rs786204023
|
Disease |
Methylenetetrahydrofolate reductase deficiency (MTHFRD) [MIM:236250] |
|
rs786204024
|
Disease |
Methylenetetrahydrofolate reductase deficiency (MTHFRD) [MIM:236250] |
|
rn00680
|
Methane metabolism
|
|
dbSNP |
Type |
Disease name |
|
rs1041969
|
Polymorphism |
- |
|
rs104894035
|
Disease |
Phosphoserine phosphatase deficiency (PSPHD) [MIM:614023] |
|
rs104894036
|
Disease |
Phosphoserine phosphatase deficiency (PSPHD) [MIM:614023] |
|
rs115014558
|
Polymorphism |
- |
|
rs121908520
|
Disease |
Hyperoxaluria primary 1 (HP1) [MIM:259900] |
|
rs121908524
|
Disease |
Hyperoxaluria primary 1 (HP1) [MIM:259900] |
|
rs121908527
|
Disease |
Hyperoxaluria primary 1 (HP1) [MIM:259900] |
|
rs121908530
|
Disease |
Hyperoxaluria primary 1 (HP1) [MIM:259900] |
|
rs121964925
|
Disease |
Erythrocytosis, familial, 8 (ECYT8) [MIM:222800] |
|
rs1229984
|
Polymorphism |
- |
|
rs13408961
|
Polymorphism |
- |
|
rs140992177
|
Polymorphism |
- |
|
rs180177155
|
Disease |
Hyperoxaluria primary 1 (HP1) [MIM:259900] |
|
rs180177156
|
Disease |
Hyperoxaluria primary 1 (HP1) [MIM:259900] |
|
rs180177157
|
Disease |
Hyperoxaluria primary 1 (HP1) [MIM:259900] |
|
rs180177173
|
Disease |
Hyperoxaluria primary 1 (HP1) [MIM:259900] |
|
rs180177185
|
Disease |
Hyperoxaluria primary 1 (HP1) [MIM:259900] |
|
rs180177197
|
Disease |
Hyperoxaluria primary 1 (HP1) [MIM:259900] |
|
rs180177225
|
Disease |
Hyperoxaluria primary 1 (HP1) [MIM:259900] |
|
rs180177236
|
Disease |
Hyperoxaluria primary 1 (HP1) [MIM:259900] |
|
rs180177244
|
Disease |
Hyperoxaluria primary 1 (HP1) [MIM:259900] |
|
rs180177253
|
Disease |
Hyperoxaluria primary 1 (HP1) [MIM:259900] |
|
rs180177264
|
Disease |
Hyperoxaluria primary 1 (HP1) [MIM:259900] |
|
rs180177289
|
Disease |
Hyperoxaluria primary 1 (HP1) [MIM:259900] |
|
rs180177290
|
Disease |
Hyperoxaluria primary 1 (HP1) [MIM:259900] |
|
rs2066702
|
Polymorphism |
- |
|
rs267606947
|
Disease |
Phosphoglycerate dehydrogenase deficiency (PHGDHD) [MIM:601815] |
|
rs267606949
|
Disease |
Phosphoglycerate dehydrogenase deficiency (PHGDHD) [MIM:601815] |
|
rs28730628
|
Polymorphism |
- |
|
rs34885252
|
Polymorphism |
- |
|
rs35385902
|
Polymorphism |
- |
|
rs4426527
|
Polymorphism |
- |
|
rs73106685
|
Polymorphism |
- |
|
rs751972865
|
Disease |
Erythrocytosis, familial, 8 (ECYT8) [MIM:222800] |
|
rs782308462
|
Disease |
Epileptic encephalopathy, early infantile, 51 (EIEE51) [MIM:617339] |
|
rs796052061
|
Disease |
Hyperoxaluria primary 1 (HP1) [MIM:259900] |
|
rn00710
|
Carbon fixation in photosynthetic organisms
|
|
dbSNP |
Type |
Disease name |
|
-
|
Disease |
Phosphoglycerate kinase 1 deficiency (PGK1D) [MIM:300653] |
|
rs115014558
|
Polymorphism |
- |
|
rs13408961
|
Polymorphism |
- |
|
rs137852530
|
Polymorphism |
- |
|
rs137852533
|
Disease |
Phosphoglycerate kinase 1 deficiency (PGK1D) [MIM:300653] |
|
rs140992177
|
Polymorphism |
- |
|
rs16952692
|
Polymorphism |
- |
|
rs180177155
|
Disease |
Hyperoxaluria primary 1 (HP1) [MIM:259900] |
|
rs180177156
|
Disease |
Hyperoxaluria primary 1 (HP1) [MIM:259900] |
|
rs180177157
|
Disease |
Hyperoxaluria primary 1 (HP1) [MIM:259900] |
|
rs180177173
|
Disease |
Hyperoxaluria primary 1 (HP1) [MIM:259900] |
|
rs180177197
|
Disease |
Hyperoxaluria primary 1 (HP1) [MIM:259900] |
|
rs180177225
|
Disease |
Hyperoxaluria primary 1 (HP1) [MIM:259900] |
|
rs180177244
|
Disease |
Hyperoxaluria primary 1 (HP1) [MIM:259900] |
|
rs180177264
|
Disease |
Hyperoxaluria primary 1 (HP1) [MIM:259900] |
|
rs180177290
|
Disease |
Hyperoxaluria primary 1 (HP1) [MIM:259900] |
|
rs34885252
|
Polymorphism |
- |
|
rs4426527
|
Polymorphism |
- |
|
rs73106685
|
Polymorphism |
- |
|
rs782308462
|
Disease |
Epileptic encephalopathy, early infantile, 51 (EIEE51) [MIM:617339] |
|
rs796052061
|
Disease |
Hyperoxaluria primary 1 (HP1) [MIM:259900] |
|
rn00720
|
Carbon fixation pathways in prokaryotes
|
|
dbSNP |
Type |
Disease name |
|
rs104886492
|
Unclassified |
HDS10 mitochondrial disease (HSD10MD) [MIM:300438] |
|
rs1057519906
|
Polymorphism |
- |
|
rs120074141
|
Disease |
3-ketothiolase deficiency (3KTD) [MIM:203750] |
|
rs121913499
|
Unclassified |
A glioma sample |
|
rs121913502
|
Disease |
D-2-hydroxyglutaric aciduria 2 (D2HGA2) [MIM:613657] |
|
rs1357271377
|
Unclassified |
A colorectal cancer sample |
|
rs137853096
|
Disease |
D-bifunctional protein deficiency (DBPD) [MIM:261515] |
|
rs137853101
|
Disease |
3-alpha-hydroxyacyl-CoA dehydrogenase deficiency (HADH deficiency) [MIM:231530] |
|
rs137853102
|
Disease |
3-alpha-hydroxyacyl-CoA dehydrogenase deficiency (HADH deficiency) [MIM:231530] |
|
rs141210410
|
Disease |
Combined immunodeficiency and megaloblastic anemia with or without hyperhomocysteinemia (CIMAH) [MIM:617780] |
|
rs1555336810
|
Disease |
Combined immunodeficiency and megaloblastic anemia with or without hyperhomocysteinemia (CIMAH) [MIM:617780] |
|
rs1555337681
|
Disease |
Combined immunodeficiency and megaloblastic anemia with or without hyperhomocysteinemia (CIMAH) [MIM:617780] |
|
rs1950902
|
Polymorphism |
- |
|
rs28940589
|
Disease |
Pyruvate carboxylase deficiency (PC deficiency) [MIM:266150] |
|
rs28940590
|
Disease |
Pyruvate carboxylase deficiency (PC deficiency) [MIM:266150] |
|
rs34181110
|
Disease |
Neural tube defects, folate-sensitive (NTDFS) [MIM:601634] |
|
rs370444838
|
Disease |
Combined immunodeficiency and megaloblastic anemia with or without hyperhomocysteinemia (CIMAH) [MIM:617780] |
|
rs782308462
|
Disease |
Epileptic encephalopathy, early infantile, 51 (EIEE51) [MIM:617339] |
|
hsa00730
|
Thiamine metabolism
|
|
dbSNP |
Type |
Disease name |
|
rs1048994
|
Polymorphism |
- |
|
rs371271054
|
Disease |
Thiamine metabolism dysfunction syndrome 5, episodic encephalopathy type (THMD5) [MIM:614458] |
|
hsa00740
|
Riboflavin metabolism
|
|
dbSNP |
Type |
Disease name |
|
rs1050916
|
Polymorphism |
- |
|
rs1270571213
|
Disease |
Interstitial nephritis, karyomegalic (KMIN) [MIM:614817] |
|
rs751703979
|
Disease |
Interstitial nephritis, karyomegalic (KMIN) [MIM:614817] |
|
hsa00760
|
Nicotinate and nicotinamide metabolism
|
|
dbSNP |
Type |
Disease name |
|
-
|
Disease |
Succinic semialdehyde dehydrogenase deficiency (SSADHD) [MIM:271980] |
|
-
|
Disease |
Leber congenital amaurosis 9 (LCA9) [MIM:608553] |
|
-
|
Disease |
Interstitial nephritis, karyomegalic (KMIN) [MIM:614817] |
|
rs104894452
|
Disease |
Purine nucleoside phosphorylase deficiency (PNPD) [MIM:613179] |
|
rs1244511644
|
Disease |
Leber congenital amaurosis 9 (LCA9) [MIM:608553] |
|
rs1270571213
|
Disease |
Interstitial nephritis, karyomegalic (KMIN) [MIM:614817] |
|
rs1326526453
|
Disease |
Succinic semialdehyde dehydrogenase deficiency (SSADHD) [MIM:271980] |
|
rs138613460
|
Disease |
Leber congenital amaurosis 9 (LCA9) [MIM:608553] |
|
rs145087265
|
Disease |
Succinic semialdehyde dehydrogenase deficiency (SSADHD) [MIM:271980] |
|
rs370273690
|
Disease |
Glucocorticoid deficiency 4 with or without mineralocorticoid deficiency (GCCD4) [MIM:614736] |
|
rs375628463
|
Disease |
Succinic semialdehyde dehydrogenase deficiency (SSADHD) [MIM:271980] |
|
rs387907234
|
Disease |
Glucocorticoid deficiency 4 with or without mineralocorticoid deficiency (GCCD4) [MIM:614736] |
|
rs387907291
|
Disease |
Leber congenital amaurosis 9 (LCA9) [MIM:608553] |
|
rs387907293
|
Disease |
Leber congenital amaurosis 9 (LCA9) [MIM:608553] |
|
rs62621664
|
Polymorphism |
- |
|
rs72552283
|
Disease |
Succinic semialdehyde dehydrogenase deficiency (SSADHD) [MIM:271980] |
|
rs751703979
|
Disease |
Interstitial nephritis, karyomegalic (KMIN) [MIM:614817] |
|
rs761948762
|
Disease |
Leber congenital amaurosis 9 (LCA9) [MIM:608553] |
|
rs763325435
|
Disease |
Leber congenital amaurosis 9 (LCA9) [MIM:608553] |
|
rs765561257
|
Disease |
Succinic semialdehyde dehydrogenase deficiency (SSADHD) [MIM:271980] |
|
rs771336246
|
Disease |
Leber congenital amaurosis 9 (LCA9) [MIM:608553] |
|
rs864309721
|
Disease |
Takenouchi-Kosaki syndrome (TKS) [MIM:616737] |
|
hsa00770
|
Pantothenate and CoA biosynthesis
|
|
dbSNP |
Type |
Disease name |
|
-
|
Disease |
Neurodegeneration with brain iron accumulation 1 (NBIA1) [MIM:234200] |
|
rs1270571213
|
Disease |
Interstitial nephritis, karyomegalic (KMIN) [MIM:614817] |
|
rs137852959
|
Disease |
Neurodegeneration with brain iron accumulation 1 (NBIA1) [MIM:234200] |
|
rs137852962
|
Disease |
Neurodegeneration with brain iron accumulation 1 (NBIA1) [MIM:234200] |
|
rs45523444
|
Polymorphism |
- |
|
rs45562238
|
Polymorphism |
- |
|
rs45624336
|
Polymorphism |
- |
|
rs751703979
|
Disease |
Interstitial nephritis, karyomegalic (KMIN) [MIM:614817] |
|
hsa00790
|
Folate biosynthesis
|
|
dbSNP |
Type |
Disease name |
|
-
|
Disease |
Phenylketonuria (PKU) [MIM:261600] |
|
-
|
Disease |
46,XY sex reversal 8 (SRXY8) [MIM:614279] |
|
rs1048994
|
Polymorphism |
- |
|
rs1056892
|
Polymorphism |
- |
|
rs11545078
|
Polymorphism |
- |
|
rs118203925
|
Disease |
Non-phenylketonuria hyperphenylalaninemia (Non-PKU HPA) [MIM:261600] |
|
rs121908605
|
Disease |
Molybdenum cofactor deficiency, complementation group B (MOCODB) [MIM:252160] |
|
rs1328320990
|
Disease |
Hyperphenylalaninemia, BH4-deficient, A (HPABH4A) [MIM:261640] |
|
rs1486763160
|
Disease |
Phenylketonuria (PKU) [MIM:261600] |
|
rs199475567
|
Disease |
Phenylketonuria (PKU) [MIM:261600] |
|
rs199475579
|
Disease |
Phenylketonuria (PKU) [MIM:261600] |
|
rs199475580
|
Disease |
Phenylketonuria (PKU) [MIM:261600] |
|
rs199475582
|
Disease |
Phenylketonuria (PKU) [MIM:261600] |
|
rs199475598
|
Disease |
Hyperphenylalaninemia (HPA) [MIM:261600] |
|
rs199475610
|
Disease |
Phenylketonuria (PKU) [MIM:261600] |
|
rs199475643
|
Disease |
Hyperphenylalaninemia (HPA) [MIM:261600] |
|
rs199475651
|
Disease |
Phenylketonuria (PKU) [MIM:261600] |
|
rs2233213
|
Polymorphism |
- |
|
rs2233215
|
Polymorphism |
- |
|
rs2233218
|
Polymorphism |
- |
|
rs2835285
|
Polymorphism |
- |
|
rs387906619
|
Disease |
Megaloblastic anemia due to dihydrofolate reductase deficiency (DHFRD) [MIM:613839] |
|
rs5030841
|
Disease |
Phenylketonuria (PKU) [MIM:261600] |
|
rs5030842
|
Disease |
Phenylketonuria (PKU) [MIM:261600] |
|
rs5030847
|
Disease |
Phenylketonuria (PKU) [MIM:261600] |
|
rs5030851
|
Disease |
Phenylketonuria (PKU) [MIM:261600] |
|
rs62507340
|
Disease |
Phenylketonuria (PKU) [MIM:261600] |
|
rs62507347
|
Disease |
Non-phenylketonuria hyperphenylalaninemia (Non-PKU HPA) [MIM:261600] |
|
rs62508578
|
Disease |
Phenylketonuria (PKU) [MIM:261600] |
|
rs62508580
|
Disease |
Phenylketonuria (PKU) [MIM:261600] |
|
rs62508588
|
Disease |
Non-phenylketonuria hyperphenylalaninemia (Non-PKU HPA) [MIM:261600] |
|
rs62508694
|
Disease |
Phenylketonuria (PKU) [MIM:261600] |
|
rs62508698
|
Disease |
Phenylketonuria (PKU) [MIM:261600] |
|
rs62514902
|
Disease |
Phenylketonuria (PKU) [MIM:261600] |
|
rs62514958
|
Disease |
Phenylketonuria (PKU) [MIM:261600] |
|
rs62516062
|
Disease |
Phenylketonuria (PKU) [MIM:261600] |
|
rs62517181
|
Disease |
Phenylketonuria (PKU) [MIM:261600] |
|
rs62635346
|
Disease |
Phenylketonuria (PKU) [MIM:261600] |
|
rs62642916
|
Disease |
Phenylketonuria (PKU) [MIM:261600] |
|
rs62642918
|
Disease |
Phenylketonuria (PKU) [MIM:261600] |
|
rs62642930
|
Disease |
Phenylketonuria (PKU) [MIM:261600] |
|
rs62642934
|
Disease |
Non-phenylketonuria hyperphenylalaninemia (Non-PKU HPA) [MIM:261600] |
|
rs62642942
|
Disease |
Phenylketonuria (PKU) [MIM:261600] |
|
rs62642944
|
Disease |
Phenylketonuria (PKU) [MIM:261600] |
|
rs74503222
|
Disease |
Phenylketonuria (PKU) [MIM:261600] |
|
rs74603784
|
Disease |
Phenylketonuria (PKU) [MIM:261600] |
|
rs76394784
|
Disease |
Phenylketonuria (PKU) [MIM:261600] |
|
hsa00830
|
Retinol metabolism
|
|
dbSNP |
Type |
Disease name |
|
rs1041969
|
Polymorphism |
- |
|
rs1229984
|
Polymorphism |
- |
|
rs12721627
|
Polymorphism |
- |
|
rs12721629
|
Polymorphism |
- |
|
rs138142612
|
Polymorphism |
- |
|
rs17884712
|
Polymorphism |
- |
|
rs192154563
|
Polymorphism |
- |
|
rs2066702
|
Polymorphism |
- |
|
rs28371759
|
Polymorphism |
- |
|
rs28730628
|
Polymorphism |
- |
|
rs3208363
|
Polymorphism |
- |
|
rs35385902
|
Polymorphism |
- |
|
rs3758581
|
Polymorphism |
- |
|
rs41291556
|
Polymorphism |
- |
|
rs4986910
|
Polymorphism |
- |
|
rs4987161
|
Polymorphism |
- |
|
rs55785340
|
Polymorphism |
- |
|
rs55951658
|
Polymorphism |
- |
|
rs56199635
|
Polymorphism |
- |
|
rs56324128
|
Polymorphism |
- |
|
rs56337013
|
Polymorphism |
- |
|
rs67784355
|
Polymorphism |
- |
|
rs72552267
|
Polymorphism |
- |
|
rs72552799
|
Polymorphism |
- |
|
hsa00860
|
Porphyrin and chlorophyll metabolism
|
|
dbSNP |
Type |
Disease name |
|
-
|
Disease |
Hereditary coproporphyria (HCP) [MIM:121300] |
|
-
|
Disease |
Hepatoerythropoietic porphyria (HEP) [MIM:176100] |
|
-
|
Disease |
Protoporphyria, erythropoietic, 1 (EPP1) [MIM:177000] |
|
-
|
Disease |
Congenital erythropoietic porphyria (CEP) [MIM:263700] |
|
rs1050916
|
Polymorphism |
- |
|
rs1055019947
|
Disease |
Protoporphyria, erythropoietic, 1 (EPP1) [MIM:177000] |
|
rs11541962
|
Polymorphism |
- |
|
rs11541963
|
Polymorphism |
- |
|
rs12144752
|
Polymorphism |
- |
|
rs121908014
|
Disease |
Congenital erythropoietic porphyria (CEP) [MIM:263700] |
|
rs121908020
|
Disease |
Congenital erythropoietic porphyria (CEP) [MIM:263700] |
|
rs121908021
|
Disease |
Congenital erythropoietic porphyria (CEP) [MIM:263700] |
|
rs121917866
|
Disease |
Hereditary coproporphyria (HCP) [MIM:121300] |
|
rs121917868
|
Disease |
Hereditary coproporphyria (HCP) [MIM:121300] |
|
rs121917872
|
Disease |
Hereditary coproporphyria (HCP) [MIM:121300] |
|
rs121917874
|
Disease |
Hereditary coproporphyria (HCP) [MIM:121300] |
|
rs121918058
|
Disease |
Familial porphyria cutanea tarda (FPCT) [MIM:176100] |
|
rs121918063
|
Disease |
Familial porphyria cutanea tarda (FPCT) [MIM:176100] |
|
rs1288116010
|
Disease |
Leukodystrophy, hypomyelinating, 15 (HLD15) [MIM:617951] |
|
rs139388833
|
Disease |
Congenital erythropoietic porphyria (CEP) [MIM:263700] |
|
rs17153561
|
Polymorphism |
- |
|
rs17173752
|
Polymorphism |
- |
|
rs201826432
|
Disease |
Hereditary coproporphyria (HCP) [MIM:121300] |
|
rs28941774
|
Disease |
Congenital erythropoietic porphyria (CEP) [MIM:263700] |
|
rs28941775
|
Disease |
Congenital erythropoietic porphyria (CEP) [MIM:263700] |
|
rs28941784
|
Disease |
Methylmalonic aciduria type cblB (MMAB) [MIM:251110] |
|
rs376128990
|
Disease |
Methylmalonic aciduria type cblB (MMAB) [MIM:251110] |
|
rs397515528
|
Disease |
Congenital erythropoietic porphyria (CEP) [MIM:263700] |
|
rs5030752
|
Polymorphism |
- |
|
rs749758687
|
Disease |
Methylmalonic aciduria type cblB (MMAB) [MIM:251110] |
|
rs759347283
|
Disease |
Hereditary coproporphyria (HCP) [MIM:121300] |
|
rs762617943
|
Disease |
Familial porphyria cutanea tarda (FPCT) [MIM:176100] |
|
rs767029901
|
Disease |
Congenital erythropoietic porphyria (CEP) [MIM:263700] |
|
rs769378741
|
Disease |
Hepatoerythropoietic porphyria (HEP) [MIM:176100] |
|
rs777433697
|
Disease |
Congenital erythropoietic porphyria (CEP) [MIM:263700] |
|
rs898824971
|
Unclassified |
Leukodystrophy, hypomyelinating, 15 (HLD15) [MIM:617951] |
|
rs982293378
|
Disease |
Familial porphyria cutanea tarda (FPCT) [MIM:176100] |
|
hsa00900
|
Terpenoid backbone biosynthesis
|
|
dbSNP |
Type |
Disease name |
|
-
|
Disease |
Porokeratosis 3, multiple types (POROK3) [MIM:175900] |
|
rs104895297
|
Disease |
Hyperimmunoglobulinemia D and periodic fever syndrome (HIDS) [MIM:260920] |
|
rs104895298
|
Disease |
Hyperimmunoglobulinemia D and periodic fever syndrome (HIDS) [MIM:260920] |
|
rs104895301
|
Disease |
Porokeratosis 3, multiple types (POROK3) [MIM:175900] |
|
rs104895301
|
Disease |
Hyperimmunoglobulinemia D and periodic fever syndrome (HIDS) [MIM:260920] |
|
rs104895314
|
Disease |
Mevalonic aciduria (MEVA) [MIM:610377] |
|