Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs4244285
rs4244285
Entrez Id: 1557
Gene Symbol: CYP2C19
CYP2C19
CUI: C1956346
Disease:
Coronary Artery Disease
0.020 GeneticVariation BEFREE In this study of patients with coronary artery disease the frequencies of the Extreme Metabolizers, Intermediate Metabolizers in CYP2C19*2 (rs4244285) were present in 90% and 10% but no Poor Metabolizers were found in this allele. 27915083 2017
dbSNP: rs4244285
rs4244285
Entrez Id: 1557
Gene Symbol: CYP2C19
CYP2C19
CUI: C1956346
Disease:
Coronary Artery Disease
0.020 GeneticVariation BEFREE The aim of this study was to investigate whether the genetic functional variant 681G>A (*2) of cytochrome CYP2C19 is associated with adverse cardiovascular outcomes in Chinese patients with coronary artery disease (CAD). 22071359 2012