rs1801282, PPARG

N. diseases: 131
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
0.070 GeneticVariation BEFREE Association between peroxisome proliferator-activated receptor γ-2 gene Pro12Ala polymorphisms and risk of hypertension: an updated meta-analysis. 30777927 2019
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
0.070 GeneticVariation BEFREE The results indicated the significant association of PPARγ2 rs1801282 polymorphism with hypertension susceptibility among East Asians. 22561695 2012
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
0.070 GeneticVariation BEFREE The Pro12Ala polymorphism of peroxisome proliferator-activated receptor-gamma (PPARgamma) has been associated with decreased obesity, insulin resistance, type 2 diabetes and other age-associated diseases such as cognitive impairment, hypertension, cancer, osteoarthritis. 19766907 2009
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
0.070 GeneticVariation BEFREE We randomly recruited 251 nuclear families (433 parents and 493 offspring) in the framework of the European Project on Genes in Hypertension study and genotyped 926 participants in whom all serum lipid variables and information on alcohol consumption were available for PPARgamma2 Pro12Ala. 15716591 2005
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
0.070 GeneticVariation BEFREE Peroxisome proliferator-activated receptor-gamma2 Pro12Ala and endothelial nitric oxide synthase-4a/b gene polymorphisms are not associated with hypertension in diabetes mellitus type 2. 15662218 2005
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
0.070 GeneticVariation BEFREE The data suggest a contribution of the Pro12Ala polymorphism of PPARgamma to genetic susceptibility to type 2 diabetes mellitus and hypertension, but not to insulin sensitivity in hypertensive subjects. 15563983 2004
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
0.070 GeneticVariation BEFREE The Pro12Ala polymorphism is not directly associated with obesity, hypertension or diabetes in this population. 11248748 2001