Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1801282
rs1801282
PPARG
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		0.050 GeneticVariation BEFREE Subgroup analysis based on disease showed that the PPARγ2 Pro12Ala (rs1801282) polymorphism was correlated with a higher risk of MI under both allelic and dominant models, while no statistical significance was found for association with CAD or ACS under allele or dominant models. 26782516

2015
dbSNP: rs1801282
rs1801282
PPARG
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		0.050 GeneticVariation BEFREE We conclude that PPARg2 Pro12Ala polymorphisms are associated with increased risk for myocardial infarction in Han Chinese in Hohhot. 22653647

2012
dbSNP: rs1801282
rs1801282
PPARG
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		0.050 GeneticVariation BEFREE We aimed to determine whether the Pro12Ala polymorphism interacts with polyunsaturated fat intake to affect the risk of myocardial infarction (MI). 17921408

2007
dbSNP: rs1801282
rs1801282
PPARG
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		0.050 GeneticVariation BEFREE Our study suggests that Pro12Ala polymorphism is associated with increased risk of MI. 16881538

2006
dbSNP: rs1801282
rs1801282
PPARG
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		0.050 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