Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs5186
rs5186
Entrez Id: 185
Gene Symbol: AGTR1
AGTR1
CUI: C0020538
Disease:
Hypertensive disease
0.060 GeneticVariation BEFREE We did not observe associations between hypertension and rs1799752 (<i>P</i>=0.422), rs699 (<i>P</i>=0.36), rs5186 (<i>P</i>=0.49), and rs1799998 (<i>P</i>=0.71). 31511791 2019
dbSNP: rs5186
rs5186
Entrez Id: 185
Gene Symbol: AGTR1
AGTR1
CUI: C0020538
Disease:
Hypertensive disease
0.060 GeneticVariation BEFREE Angiotensin II Type 1 Receptor rs5186 Gene Variant Predicts Incident NAFLD and Associated Hypertension: Role of Dietary Fat-Induced Pro-Inflammatory Cell Activation. 30920415 2019
dbSNP: rs5186
rs5186
Entrez Id: 185
Gene Symbol: AGTR1
AGTR1
CUI: C0020538
Disease:
Hypertensive disease
0.060 GeneticVariation BEFREE An association was found between rs5186, rs699, and hypertension under allele contrast and homozygous codominant models (odds ratio, 1.63 [95% confidence interval, 1.04-2.54] and 4.01 [95% confidence interval, 1.17-13.80] for rs5186, respectively; and 1.80 [95% confidence interval, 1.13-2.87] for rs699). 29520984 2018
dbSNP: rs5186
rs5186
Entrez Id: 185
Gene Symbol: AGTR1
AGTR1
CUI: C0020538
Disease:
Hypertensive disease
0.060 GeneticVariation BEFREE This study examined the SNPs AGT rs699 (Met235Thr), ADD1 rs4961 (Gly460Trp), NPPA rs5063 (Val32Met), GPX1 rs1050450 (Pro198Leu), and AGTR1 rs5186 (A1166C) in relation to hypertension and salt sensitivity. 27480094 2017
dbSNP: rs5186
rs5186
Entrez Id: 185
Gene Symbol: AGTR1
AGTR1
CUI: C0020538
Disease:
Hypertensive disease
0.060 GeneticVariation BEFREE A polymorphism in the angiotensin II type 1 receptor gene (AGTR1/rs5186) has been associated with an increased risk for arterial stiffness, hypertension, and ischemic stroke. 24981111 2014
dbSNP: rs5186
rs5186
Entrez Id: 185
Gene Symbol: AGTR1
AGTR1
CUI: C0020538
Disease:
Hypertensive disease
0.060 GeneticVariation BEFREE We assessed whether distributions of 3 single nucleotide polymorphisms in genes coding for components of G protein signaling pathways that have been associated with hypertension differ between women with preeclampsia and normotensive pregnant women; the G protein β3 subunit gene (GNB3) C825T polymorphism (rs5443), the angiotensin II type 1 receptor gene (AGTR1) 3'UTR A1166C polymorphism (rs5186), and the regulator of G protein signaling 2 gene (RGS2) 3'UTR C1114G polymorphism (rs4606). 23339167 2013