rs3764261, None

N. diseases: 26
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Age related macular degeneration
CUI: C0242383
Disease: Age related macular degeneration
0.860 GeneticVariation BEFREE Among them, CETP (rs3764261/rs2303790) and ABCG1 (rs57137919) were the major susceptibility genes for PCV in Asian population and ABCG1 (rs57137919) showed allelic diversity between PCV and AMD. 29977615 2018
Age related macular degeneration
CUI: C0242383
Disease: Age related macular degeneration
0.860 GeneticVariation BEFREE Our study identified two polymorphisms with a higher risk of AMD development (rs5882 and rs708272) and a protective polymorphism for AMD (rs3764261). 28918250 2017
Age related macular degeneration
CUI: C0242383
Disease: Age related macular degeneration
0.860 GeneticVariation BEFREE This meta-analysis revealed that both CETP rs3764261 and LIPC rs10468017 polymorphisms were significantly associated with AMD risk. 26503844 2015
Age related macular degeneration
CUI: C0242383
Disease: Age related macular degeneration
0.860 GeneticVariation BEFREE Our data suggested that the allele A in rs3764261 in CETP gene may be associated with a decreased risk of advanced AMD in Chinese population. 24498989 2015
Age related macular degeneration
CUI: C0242383
Disease: Age related macular degeneration
0.860 GeneticVariation BEFREE The SNP rs3764261 in the cholesteryl ester transfer protein (CETP) gene was associated significantly with neovascular AMD (P = 1.82×10(-4); odds ratio [OR], 1.89) and PCV (P = 4.04×10(-4); OR, 1.80). 24393350 2014
Age related macular degeneration
CUI: C0242383
Disease: Age related macular degeneration
0.860 GeneticVariation BEFREE After multivariate adjustment for age, sex, educational level, smoking, BMI, lipid-lowering medication use, cardiovascular disease and diabetes, and for all relevant genetic polymorphisms (ApoE2, ApoE4, CFH Y402H, ARMS2 A69S, LIPC rs10468017, LIPC rs493258, LPL rs12678919, ABCA1 rs1883025 and CETP rs3764261), higher HDL was significantly associated with an increased risk of early (OR = 2.45, 95%CI: 1.54-3.90; P = 0.0002) and any AMD (OR = 2.29, 95%CI: 1.46-3.59; P = 0.0003). 24608419 2014
Age related macular degeneration
CUI: C0242383
Disease: Age related macular degeneration
0.860 GeneticVariation GWASCAT Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degeneration. 21665990 2011
Age related macular degeneration
CUI: C0242383
Disease: Age related macular degeneration
0.860 GeneticVariation GWASDB Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degeneration. 21665990 2011
Age related macular degeneration
CUI: C0242383
Disease: Age related macular degeneration
0.860 GeneticVariation GWASDB Genetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to age-related macular degeneration. 20385819 2010
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
0.830 GeneticVariation BEFREE Our data support the notion that the consumption of a Mediterranean diet may play a contributing role in triggering lipid metabolism by interacting with the rs3764261 SNP at CETP gene locus in MetS patients. 28057378 2018
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
0.830 GeneticVariation BEFREE No significant interactions were found between rs3764261 and macronutrient intakes in association with MetS or its components. 29942448 2018
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
0.830 GeneticVariation BEFREE (3) The rs1800775 polymorphism was associated with high fasting blood glucose levels and low high density lipoprotein cholesterol (HDL-C); rs3764261 and rs12149545 polymorphisms were associated with all components of MS except high blood pressure; rs711752 and rs708272 polymorphisms were associated with low HDL-C (all <i>p</i> < 0.05). 28629169 2017
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
0.830 GeneticVariation GWASDB A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. 21386085 2011
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
0.830 GeneticVariation GWASCAT A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. 21386085 2011
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
0.830 GeneticVariation GWASCAT A genome-wide association study of the metabolic syndrome in Indian Asian men. 20694148 2010
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
0.830 GeneticVariation GWASDB A genome-wide association study of the metabolic syndrome in Indian Asian men. 20694148 2010
Low density lipoprotein cholesterol measurement
0.800 GeneticVariation GWASCAT Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids. 30926973 2019
High density lipoprotein measurement
0.800 GeneticVariation GWASCAT Genetic analyses of diverse populations improves discovery for complex traits. 31217584 2019
High density lipoprotein measurement
0.800 GeneticVariation GWASCAT We replicated the association of rs3764261 within CETP with HDL-C levels in the study population, and found other previously unidentified SNPs to be significant at the suggestive level, in both previously identified and unidentified genes. 31211820 2019
High density lipoprotein measurement
0.800 GeneticVariation GWASCAT Genome-wide association study of blood lipids in Indians confirms universality of established variants. 30911093 2019
Serum total cholesterol measurement
CUI: C1445957
Disease: Serum total cholesterol measurement
0.800 GeneticVariation GWASCAT Genetic analyses of diverse populations improves discovery for complex traits. 31217584 2019
High density lipoprotein measurement
0.800 GeneticVariation GWASCAT A large electronic-health-record-based genome-wide study of serum lipids. 29507422 2018
Serum total cholesterol measurement
CUI: C1445957
Disease: Serum total cholesterol measurement
0.800 GeneticVariation GWASCAT A large electronic-health-record-based genome-wide study of serum lipids. 29507422 2018
Low density lipoprotein cholesterol measurement
0.800 GeneticVariation GWASCAT A large electronic-health-record-based genome-wide study of serum lipids. 29507422 2018
Triglycerides measurement
CUI: C0202236
Disease: Triglycerides measurement
0.800 GeneticVariation GWASCAT A large electronic-health-record-based genome-wide study of serum lipids. 29507422 2018