Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs5186
rs5186
0.020 GeneticVariation BEFREE Meta-analysis showed significant associations between rs5186 in AGTR1 and increased rates by 25-34% for the primary endpoint (composite of death or nonfatal myocardial infarction, hospitalization for unstable angina, heart failure or peripheral vascular event), all-cause mortality, cardiovascular mortality and heart failure; all P < 0.001. 29982608

2019

dbSNP: rs5186
rs5186
0.020 GeneticVariation BEFREE To evaluate the impact of AGTR1 A1166C (rs5186) on the response to candesartan in patients with heart failure. 29701105

2018