Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs4539
rs4539
0.050 GeneticVariation BEFREE The rs4539 (AA), H1, H2, and H3 are genetic predictors for postoperative persistence of hypertension for Chinese patients treated by adrenalectomy with APA. 20708777

2010

dbSNP: rs4539
rs4539
0.050 GeneticVariation BEFREE To investigate the -344T/C, K173R and intron-2 conversion polymorphisms of CYP11B2 for an association with hypertension in highlanders accustomed to a high salt intake. 15643128

2005

dbSNP: rs4539
rs4539
0.050 GeneticVariation BEFREE The objective of this study was to investigate the association of polymorphisms in the aldosterone synthase gene CYP11B2 (-344T/C, Lys173/Arg, and an intronic conversion [IC]) with stage-2 hypertension in northern Han Chinese. 15479186

2004

dbSNP: rs4539
rs4539
0.050 GeneticVariation BEFREE To compare the frequency of three variants (-344C/T, intron 2 conversion, and the K173R polymorphism) of the aldosterone synthase gene in blacks and whites, and to determine any association of the variants with hypertension. 12544440

2003

dbSNP: rs4539
rs4539
0.050 GeneticVariation BEFREE Lys(173)Arg and -344T/C variants of CYP11B2 in Japanese patients with low-renin hypertension. 10720581

2000

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

dbSNP: rs542092383
rs542092383
0.010 GeneticVariation BEFREE The AG genotype frequency of SNP rs542092383 was significantly associated with an increased risk of hypertension (OR 4.513, 95% CI 1.426-14.287, P = .010). 28953657

2017

dbSNP: rs10086846
rs10086846
0.010 GeneticVariation BEFREE Of 41 SNPs genotyped, rs3789678 and rs2493132 within AGT, rs4305 within ACE, rs275645 within AGTR1, rs3802230 and rs10086846 within CYP11B2 were shown to associate with hypertension. 24015270

2013

dbSNP: rs3802230
rs3802230
0.010 GeneticVariation BEFREE Of 41 SNPs genotyped, rs3789678 and rs2493132 within AGT, rs4305 within ACE, rs275645 within AGTR1, rs3802230 and rs10086846 within CYP11B2 were shown to associate with hypertension. 24015270

2013

dbSNP: rs4536
rs4536
0.010 GeneticVariation BEFREE In the Hani minority, rs4536 was significantly associated with hypertension, after Bonferroni correction. 21127960

2011

dbSNP: rs5310
rs5310
0.010 GeneticVariation BEFREE In addition to these polymorphisms, the T(-344)C polymorphism in the promoter of the aldosterone synthase gene (CYP11B2) and the C825T polymorphism of the G-protein beta3 subunit gene (GNB3) are considered candidates for the genetic risk of salt-sensitive hypertension. 12924618

2003