rs3856806, PPARG

N. diseases: 41
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
0.060 GeneticVariation BEFREE Risk analysis of Kazakhs revealed that individuals with the CT and TT genotypes at rs3856806 had an increased risk, 0.524- and 0.770-fold, respectively, of developing MS than those possessing the CC genotype. 26125830 2015
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
0.060 GeneticVariation BEFREE This study suggests that the PPARγ C1431T polymorphism is related to an increased risk of MetS in an Iranian population and interacts with the Pro12Ala polymorphism, further increasing the risk of MetS. 24464185 2014
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
0.060 GeneticVariation BEFREE The influences of PPARγ (C1431T and Pro12Ala) and RBP4 (-803GA) polymorphisms on metabolic syndrome in HIV-infected patients receiving anti-retroviral therapy were examined in this study. 23145084 2012
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
0.060 GeneticVariation BEFREE Two-way ANCOVA with adjustment for age as a covariate indicated that fitness and the CC genotype of C1431T in the PPARγ2 gene interacted to produce a significant effect on MetS risk in younger men and that the risk of MetS in the CC genotype group with low cardiorespiratory fitness was significantly higher than that in the corresponding CT+TT genotypes or in the high fitness groups. 21156835 2011
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
0.060 GeneticVariation BEFREE C1431T, but not Pro12Ala polymorphisms, are associated with MS in a Chinese population. 19237017 2009
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
0.060 GeneticVariation BEFREE Further analyses stratified on the 1431C>T single nucleotide polymorphism (SNP) indicated that the rare alleles of the P2 -689C>T and Pro12Ala SNPs were associated with an increased risk of the metabolic syndrome when combined to the 1431CC genotype. 16186413 2005