Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs5186
rs5186
0.030 GeneticVariation BEFREE The gain-of-function rs5186 A1166C variant in angtiotensin receptor type 1 (AGTR1) gene has been linked to hypertension, cardiovascular disease and metabolic syndrome. 30920415

2019

dbSNP: rs5186
rs5186
0.030 GeneticVariation BEFREE In postmenopausal women, an increased MetS risk was found for the ADRB2 rs180088 (OR 1.28, 95% CI 0.99-1.65), PAI1 rs1799768 (OR 1.07, 95% CI 1.01-1.14), SCNN1A rs5742912 (OR 1.22, 95% CI 1.01-1.47), and IL1A rs1800587 (OR 1.07, 95% CI 1.01-1.15), whereas the AGTR1 rs5186 (OR 0.93, 95% CI 0.87-0.99) was associated with decreased risk. 19619703

2009

dbSNP: rs5186
rs5186
0.030 GeneticVariation BEFREE Metabolic syndrome trait associations were strongest for the 3' block generally and for the C allele of rs5186:A>C specifically. 17211857

2007