PRDX1, peroxiredoxin 1, 5052

N. diseases: 237; N. variants: 3
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs4660306
rs4660306
Entrez Id: 5052;25974
Gene Symbol: PRDX1;MMACHC
PRDX1;MMACHC
CUI: C2242817
Disease:
Homocysteine measurement 		T 0.800 GeneticVariation GWASDB Common genetic loci influencing plasma homocysteine concentrations and their effect on risk of coronary artery disease. 23824729 2013
dbSNP: rs4660306
rs4660306
Entrez Id: 5052;25974
Gene Symbol: PRDX1;MMACHC
PRDX1;MMACHC
CUI: C2242817
Disease:
Homocysteine measurement 		T 0.800 GeneticVariation GWASCAT Common genetic loci influencing plasma homocysteine concentrations and their effect on risk of coronary artery disease. 23824729 2013
dbSNP: rs1379672870
rs1379672870
Entrez Id: 5052;25974
Gene Symbol: PRDX1;MMACHC
PRDX1;MMACHC
CUI: C4693974
Disease:
METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblC TYPE, DIGENIC 		A 0.700 CausalMutation CLINVAR
dbSNP: rs751828470
rs751828470
Entrez Id: 5052;25974
Gene Symbol: PRDX1;MMACHC
PRDX1;MMACHC
CUI: C4693974
Disease:
METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblC TYPE, DIGENIC 		A 0.700 CausalMutation CLINVAR