Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1805192
rs1805192
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.090 GeneticVariation BEFREE Our results suggest that the Pro12Ala, C161T and C1431T polymorphisms of PPARG gene are not associated with CHD susceptibility. 23065280

2013

dbSNP: rs1805192
rs1805192
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.090 GeneticVariation BEFREE Association of the PPARG Pro12Ala polymorphism with type 2 diabetes and incident coronary heart disease in a Hong Kong Chinese population. 22515931

2012

dbSNP: rs1805192
rs1805192
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.090 GeneticVariation BEFREE The Pro12Ala polymorphism in the peroxisome proliferator-activated receptor gamma-2 gene (PPARγ2) is associated with increased risk of coronary artery disease: a meta-analysis. 23300871

2012

dbSNP: rs1805192
rs1805192
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.090 GeneticVariation BEFREE But PPARG P12A polymorphism is not associated with CHD risk. 22987045

2012

dbSNP: rs1805192
rs1805192
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.090 GeneticVariation BEFREE Our findings shows the association of these two polymorphisms with serum triglyceride levels, which was increased in the order of P12P-CC < P12P-CT < P12A-CC < P12A-CT in the CHD patients with diabetes. 21833536

2011

dbSNP: rs1805192
rs1805192
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.090 GeneticVariation BEFREE Homozygosity for the Ala allele of the PPARγ2 Pro12Ala polymorphism is associated with reduced risk of coronary artery disease. 21206011

2010

dbSNP: rs1805192
rs1805192
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.090 GeneticVariation BEFREE The aim was to investigate if the polymorphism PPARgamma2 Pro12Ala, which encodes a less efficient transcription factor, was associated with risk of acute coronary disease and if there were interactions between this polymorphism and factors that modify PPARgamma activity, such as alcohol intake, smoking, and use of non-steroidal anti-inflammatory medicine. 19500413

2009

dbSNP: rs1805192
rs1805192
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.090 GeneticVariation BEFREE No association of Pro12Ala polymorphism of PPAR-gamma gene with coronary artery disease in Korean subjects. 17322631

2007

dbSNP: rs1805192
rs1805192
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.090 GeneticVariation BEFREE The potential interaction between PPARG2 P12A, overweight, and increased CHD risk needs further evaluation. 15920035

2005