Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2619112
rs2619112
Entrez Id: 246
Gene Symbol: ALOX15
ALOX15
CUI: C1956346
Disease:
Coronary Artery Disease
0.020 GeneticVariation BEFREE The present study shows that rs7217186:C > T and rs2619112:G > A of ALOX15 are associated with increased risk of CAD in the North Indian population. 29068244 2018
dbSNP: rs2619112
rs2619112
Entrez Id: 246
Gene Symbol: ALOX15
ALOX15
CUI: C1956346
Disease:
Coronary Artery Disease
0.020 GeneticVariation BEFREE The carriers of the C allele (the CC homozygote and the CT heterozygote) of rs7217186:T>C and the carriers of the A allele (the AA homozygote and the GA heterozygote) of rs2619112</span>:G>A displayed elevated odds ratios (ORs) for CAD compared with the TT homozygotes and GG homozygotes, respectively, after adjusting for other potential confounders including age, sex, body mass index, systolic blood pressure, diastolic blood pressure, glucose, triglyceride, total cholesterol, high-density lipoprotein cholesterol, low-density lipoprotein cholesterol, and smoking status (adjusted odds ratio [OR] = 3.2, 95% confidence interval [CI]: 1.335-7.665, P = 0.009 and adjusted OR = 3.5, 95% CI: 1.343-9.330, P = 0.011). 20676957 2010