rs3764261, None

N. diseases: 26
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
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