Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs708272
rs708272
Entrez Id: 1071
Gene Symbol: CETP
CETP
CUI: C0027051
Disease:
Myocardial Infarction
0.030 GeneticVariation BEFREE Thus, rs708272 is associated with myocardial infarction in the white population of Western Siberia (Russia). 31739638 2019
dbSNP: rs708272
rs708272
Entrez Id: 1071
Gene Symbol: CETP
CETP
CUI: C0027051
Disease:
Myocardial Infarction
0.030 GeneticVariation BEFREE The current meta-analysis suggests that CETP rs708272 (C>T) and rs1800775 (C>A) polymorphisms may contribute to MI</span> susceptibility, especially among Caucasians. 24533069 2014
dbSNP: rs708272
rs708272
Entrez Id: 1071
Gene Symbol: CETP
CETP
CUI: C0027051
Disease:
Myocardial Infarction
0.030 GeneticVariation BEFREE For example, SNP rs708272 in the CETP gene was associated with a per-allele increase in HDL-C levels of 3.1 mg/dL and a concordant 24% lower risk of future myocardial infarction (age-adjusted hazard ratio, 0.76; 95% CI, 0.62 to 0.94), consistent with recent meta-analysis. 20031564 2009
dbSNP: rs17231896
rs17231896
Entrez Id: 1071
Gene Symbol: CETP
CETP
CUI: C0027051
Disease:
Myocardial Infarction
0.010 GeneticVariation BEFREE Further analysis with the inclusions of gene-gene and gene-environmental interactions shows interactions between rs17231896 (CETP) and rs17222772 (ALOX); rs17231896 (CETP) and gender. rs17237890 (CETP) and rs2070744 (NOS3) are found to be significantly associated with risks of MI adjusted by both SNPs and environmental factors. 28906356 2017
dbSNP: rs17237890
rs17237890
Entrez Id: 1071
Gene Symbol: CETP
CETP
CUI: C0027051
Disease:
Myocardial Infarction
0.010 GeneticVariation BEFREE Further analysis with the inclusions of gene-gene and gene-environmental interactions shows interactions between rs17231896 (CETP) and rs17222772 (ALOX); rs17231896 (CETP) and gender. rs17237890 (CETP) and rs2070744 (NOS3) are found to be significantly associated with risks of MI adjusted by both SNPs and environmental factors. 28906356 2017
dbSNP: rs1800775
rs1800775
Entrez Id: 1071
Gene Symbol: CETP
CETP
CUI: C0027051
Disease:
Myocardial Infarction
0.010 GeneticVariation BEFREE The current meta-analysis suggests that CETP rs708272 (C>T) and rs1800775 (C>A) polymorphisms may contribute to MI</span> susceptibility, especially among Caucasians. 24533069 2014
dbSNP: rs5882
rs5882
Entrez Id: 1071
Gene Symbol: CETP
CETP
CUI: C0027051
Disease:
Myocardial Infarction
0.010 GeneticVariation BEFREE We determined relationships between the CETP -629C-->A promoter (n = 8141), the TaqIB (n = 8289), and the I405V (n = 8265) polymorphisms, serum lipids, C-reactive protein, and clinical factors with incident coronary heart disease (defined as death from or hospitalization for myocardial infarction, ischemic heart disease, or coronary intervention) during a median of 4.94 yr follow-up. 16684835 2006
dbSNP: rs1800774
rs1800774
Entrez Id: 1071
Gene Symbol: CETP
CETP
CUI: C0027051
Disease:
Myocardial Infarction
0.010 GeneticVariation BEFREE SNPs in the 5' haploblock were significantly associated with HDL cholesterol while SNPs in the 3' haploblock were, at best, only weakly associated with HDL-C. One SNP in the 3' haploblock (rs1800774 in intron 12) was highly associated with history of myocardial infarction even though it was not associated with HDL-C. 15939053 2005
dbSNP: rs2303790
rs2303790
Entrez Id: 1071
Gene Symbol: CETP
CETP
CUI: C0027051
Disease:
Myocardial Infarction
0.010 GeneticVariation BEFREE The gene mutation frequencies of D442G in the MI, stroke and control group were 3.5%, 3.6% and 5%, respectively, and the frequencies of I 14A were 1.05%, 0.91% and 1%, respectively. 11940367 2002