Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1799998
rs1799998
0.040 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: rs1799998
rs1799998
0.040 GeneticVariation BEFREE The CC of rs4994 and CC or C allele of rs1799998 might be protective genetic factors of hypertension. 25099490

2014

dbSNP: rs1799998
rs1799998
0.040 GeneticVariation BEFREE Hypertension association reached genome-wide significance for the two variants, specifically, P=7.3 × 10(-10) for AGT rs699 and P=3.9 × 10(-8) for CYP11B2 rs1799998. 22456346

2012

dbSNP: rs1799998
rs1799998
0.040 GeneticVariation BEFREE In the present case-control study we investigated the association of -344C/T (rs1799998) [corrected] polymorphism in the promoter region of the human aldosterone (CYP11B2) gene with genetic predisposition to hypertension, ischemic stroke and stroke subtypes classified according to TOAST (Trial of Org 10172 in Acute Stroke Treatment) classification. 20598712

2010