Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs891511
rs891511
A 0.700 GeneticVariation GWASCAT Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci. 27618448

2016

dbSNP: rs1799983
rs1799983
0.100 GeneticVariation BEFREE However, a subgroup analysis adjusted with various cardiovascular risk factors confirmed positive association of the -786T>C polymorphism in CAD patients with hypertension and a smoking history and also a significant association of the intron 4 genotypes with a smoking history, but no significance has been found in the eNOS polymorphisms of 894G>T upon any risk adjustment. 16842840

2007

dbSNP: rs1799983
rs1799983
0.100 GeneticVariation BEFREE Association of endothelial nitric oxide synthase (eNOS) gene G894T polymorphism with hypertension risk and complications. 27557897

2016

dbSNP: rs1799983
rs1799983
0.100 GeneticVariation BEFREE Further studies are needed to reveal the usefulness of G894T polymorphism in hyper</span>tension risk assessment in obese. 26579574

2015

dbSNP: rs1799983
rs1799983
0.100 GeneticVariation BEFREE The Glu298Asp, T786C and 4a/4b genetic polymorphisms within the endothelial nitric oxide synthase (e-NOS) gene may predispose to hypertension, ischaemic heart disease and renal damage, possibly by reducing the generation of nitric oxide (NO), a fundamental substance in renal and cardiovascular biology. 17563560

2007

dbSNP: rs1799983
rs1799983
0.100 GeneticVariation BEFREE These results suggested no association between the Glu298Asp gene polymorphism and the incidence of hypertension in this selected population. 15475025

2004

dbSNP: rs1799983
rs1799983
0.100 GeneticVariation BEFREE The polymorphism Glu298Asp of endothelial nitric oxide (eNOS) gene has been associated with hypertension and coronary artery disease in several populations worldwide, but results are still controversial. 20083095

2010

dbSNP: rs1799983
rs1799983
0.100 GeneticVariation BEFREE The relevance of the Glu298Asp polymorphism to hypertension in this population was tested in 2 ways. 10205226

1999

dbSNP: rs1799983
rs1799983
0.100 GeneticVariation BEFREE Studies on the associations between the nitric oxide synthase gene (NOS3) Glu298Asp polymorphism and hypertension status or blood pressure (BP) levels have had inconsistent results. 15505116

2004

dbSNP: rs1799983
rs1799983
0.100 GeneticVariation BEFREE The genotypic distribution of the Met235Thr (AGT) and Glu298Asp (NOS3) polymorphisms demonstrated that both are independent risk factors of hypertension (p=0.02 and p=0.008, respectively). 22791701

2013

dbSNP: rs1799983
rs1799983
0.100 GeneticVariation BEFREE The AGT M235T and eNOS G894T polymorphisms are unlikely to play an important role in the pathogenesis of hypertension in Malays. 17977523

2008

dbSNP: rs1799983
rs1799983
0.100 GeneticVariation BEFREE A meta-analysis of 35 genetic association studies that examined the relation between hypertension and the G894T, 4a/b, T786C, and G23T polymorphisms of the endothelial nitric oxide synthase gene was carried out. 16940230

2006

dbSNP: rs1799983
rs1799983
0.100 GeneticVariation BEFREE Genotype frequencies for the -786T/C, 4b/4a, and 894G/T polymorphisms differed significantly (P<0.001) between patients and controls and were associated with an increased risk of hypertension (OR=2.0, OR=3.8, OR=1.6, respectively). 18325347

2008

dbSNP: rs1799983
rs1799983
0.100 GeneticVariation BEFREE Relation of the Glu298Asp polymorphism of the nitric oxide synthase gene to hypertension and serum cholesterol in Japanese workers. 18550157

2008

dbSNP: rs1799983
rs1799983
0.100 GeneticVariation BEFREE The aim of our study is to investigate whether genetic polymorphisms in the endothelial nitric oxide synthase (eNOS) gene (in the promoter region T(-786)C, in exon 7 (Glu298Asp) and in intron 4 (4b/4a)) or eNOS haplotypes are associated with hypertension in obese children and adolescents. 20661250

2011

dbSNP: rs1799983
rs1799983
0.100 GeneticVariation BEFREE No differences were observed in the distribution of G894T (Glu298Asp) NOS3 genotypes between the resistant hypertension group and the controlled hypertension patients. 19650939

2009

dbSNP: rs1799983
rs1799983
0.100 GeneticVariation BEFREE Overall, our findings suggest that eNOS G894T and T-786C SNPs were both significantly correlated with hypertension</span>. 28287883

2017

dbSNP: rs1799983
rs1799983
0.100 GeneticVariation BEFREE Multiple logistic regression revealed that the most predictive independent risk factor for coronary spasm was the T-786-->C mutation (P < 0.001), followed by cigarette smoking (P < 0.001), hypertension (P = 0.004), and the Glu298Asp variant (P = 0.028). 10979242

2000

dbSNP: rs1799983
rs1799983
0.100 GeneticVariation BEFREE These results do not support the hypothesis that the E298D polymorphism contributes to the genetic susceptibility to hypertension. 15942458

2005

dbSNP: rs1799983
rs1799983
0.100 GeneticVariation BEFREE In addition, a missense Glu298Asp mutation in exon 7 of the eNOS gene is reported to be a risk factor for hypertension or myocardial infarction. 12701818

2003

dbSNP: rs1799983
rs1799983
0.100 GeneticVariation BEFREE We, via a comprehensive meta-analysis, ascertained the role of eNOS G894T and 4b/a polymorphisms on hypertension in Asians, and T-786C polymorphism in Whites. 21912683

2011

dbSNP: rs1799983
rs1799983
0.100 GeneticVariation BEFREE Recently, a G894T polymorphism in exon 7 of the eNOS gene has been reported to be associated with high blood pressure. 18164968

2008

dbSNP: rs1799983
rs1799983
0.100 GeneticVariation BEFREE The NOS3 -786 T/C (SNP id rs2070744; http://www.ensembl.org ), intron 4 variable number tandem repeat (VNTR), and Glu298Asp (SNP id rs1799983) polymorphisms, have been associated with differences in NO plasma concentrations and with the risk of hypertension (HT) and ischemic cardiac disease. 21293869

2011

dbSNP: rs1799983
rs1799983
0.100 GeneticVariation BEFREE The relationship between the G894T polymorphism and hypertension in Han Chinese may be attributed to the difference in geographic background of subjects. 24846690

2015

dbSNP: rs1799983
rs1799983
0.100 GeneticVariation BEFREE We revealed that a combination of the Arg16Gly and Glu298Asp polymorphisms in ADRB2 and NOS3, respectively, remarkably increased the risk for hypertension in middle-aged and elderly humans. 19373110

2009