SLC23A2, solute carrier family 23 member 2, 9962

N. diseases: 46; N. variants: 10
Disease: Acute Coronary Syndrome ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1776964
rs1776964
Entrez Id: 9962
Gene Symbol: SLC23A2
SLC23A2
CUI: C0948089
Disease:
Acute Coronary Syndrome 		0.010 GeneticVariation BEFREE We tested the hypothesis that candidate variations rs6139591 and rs1776964 in the gene coding for sodium-dependent vitamin C transporter 2 are associated with development of acute coronary syndrome. 23990905 2013
dbSNP: rs6139591
rs6139591
Entrez Id: 9962
Gene Symbol: SLC23A2
SLC23A2
CUI: C0948089
Disease:
Acute Coronary Syndrome 		0.010 GeneticVariation BEFREE Using Cox proportional hazard models, we found that women with the rs6139591 TT genotype and a lower than median dietary vitamin C intake had a higher risk of acute coronary syndrome compared with those with the CC genotype (adjusted HR 5.39, 95% confidence interval, 2.01-14.50). 23990905 2013