Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3811951
rs3811951
Entrez Id: 5122;101929710
Gene Symbol: PCSK1;LOC101929710
PCSK1;LOC101929710
CUI: C1956346
Disease:
Coronary Artery Disease
0.010 GeneticVariation BEFREE The allele frequencies at rs3811951 were significantly different between cases and controls (30.7% vs. 37.2%), with the allele G associated with decreased risk for CAD (OR = 0.75, 95% CI = 0.59-0.94, p = 0.013). 24489861 2014
dbSNP: rs6234
rs6234
Entrez Id: 5122;101929710
Gene Symbol: PCSK1;LOC101929710
PCSK1;LOC101929710
CUI: C1956346
Disease:
Coronary Artery Disease
0.010 GeneticVariation BEFREE The SNP rs6234 was also significantly associated with CAD risk in women, with the carriers of the minor allele G at rs6234 associated with a reduced CAD risk in recessive inheritance mode (OR = 0.42, 95% CI = 0.18-0.95, p = 0.036 after adjustment). 24489861 2014