Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs5882
rs5882
Entrez Id: 1071
Gene Symbol: CETP
CETP
CUI: C1956346
Disease:
Coronary Artery Disease
0.060 GeneticVariation BEFREE Results showed that subjects with CETP rs5882 genetic variant, AA&AG genotypes, had a higher risk of developing Coronary artery disease [OR: 2.1, 95% CI (1.2-4.1), p value = 0.015]. 30902787 2019
dbSNP: rs5882
rs5882
Entrez Id: 1071
Gene Symbol: CETP
CETP
CUI: C1956346
Disease:
Coronary Artery Disease
0.060 GeneticVariation BEFREE The I405V genotype distributions were not statistically different in CAD and non-CAD groups in univariate and multivariable-adjusted logistic regression analyzes. 26773179 2016
dbSNP: rs5882
rs5882
Entrez Id: 1071
Gene Symbol: CETP
CETP
CUI: C1956346
Disease:
Coronary Artery Disease
0.060 GeneticVariation BEFREE The rs5882 polymorphism (CETP) showed a significant association and therefore could be a promising marker for CAD risk estimation while the rs708272 polymorphism had a protective effect from CAD. 26936456 2016
dbSNP: rs5882
rs5882
Entrez Id: 1071
Gene Symbol: CETP
CETP
CUI: C1956346
Disease:
Coronary Artery Disease
0.060 GeneticVariation BEFREE We studied the association of four polymorphisms (Taq1B, I405V, R451Q and A373P) in the CETP gene with lipid profile and coronary artery disease. 22854712 2012
dbSNP: rs5882
rs5882
Entrez Id: 1071
Gene Symbol: CETP
CETP
CUI: C1956346
Disease:
Coronary Artery Disease
0.060 GeneticVariation BEFREE In conclusion, the combined T allele of LIPC -514C/T and V allele of CETP I405V are associated with the risk of CAD. 19810818 2009
dbSNP: rs5882
rs5882
Entrez Id: 1071
Gene Symbol: CETP
CETP
CUI: C1956346
Disease:
Coronary Artery Disease
0.060 GeneticVariation BEFREE Cholesteryl ester transfer protein TaqIB, -629C>A and I405V polymorphisms and risk of coronary heart disease in an Indian population. 19168039 2009