rs1805192, PPARG

N. diseases: 121
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
0.060 GeneticVariation BEFREE We found a significant association between genotypes of variants in rs10865710 and rs1805192 with increased CVD risk and a potential gene-gene interaction between rs1805192 and smoking. 26475999 2016
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
0.060 GeneticVariation BEFREE Our results indicate that the Pro12Ala and C161T polymorphisms were associated with some important risk factors for CVD in HD patients in the Han Chinese population. 25096510 2014
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
0.060 GeneticVariation BEFREE To analyze the contribution of the PPAR-gamma Pro12Ala polymorphism to GH induced changes in determinants of metabolic and cardiovascular disease in short SGA children. 19808901 2010
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
0.060 GeneticVariation BEFREE Two PPARg common polymorphisms, Pro12Ala and 161C>T, have been found to be associated with cardiovascular disease. 19117570 2009
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
0.060 GeneticVariation BEFREE The Pro12Ala polymorphism in the peroxisome proliferator-activated receptor-gamma 2 gene is suggested to associate with diabetic nephropathy and cardiovascular disease in type 2 diabetes. 18467141 2008
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
0.060 GeneticVariation BEFREE Using DNA samples collected at baseline in a prospective cohort of 14 916 initially healthy American men, we evaluated a P12A polymorphism in the PPARG2 among 523 individuals who subsequently developed myocardial infarction and among 2092 individuals who remained free of reported cardiovascular disease over a mean follow-up period of 13.2 years. 12663371 2003