Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2070744
rs2070744
Entrez Id: 4846
Gene Symbol: NOS3
NOS3
CUI: C0020538
Disease:
Hypertensive disease
0.040 GeneticVariation BEFREE The C allele at rs2070744 of the NOS3 gene was shown to be significantly associated with hypertension (P=0.0443; OR=1.636). 23122309 2012
dbSNP: rs2070744
rs2070744
Entrez Id: 4846
Gene Symbol: NOS3
NOS3
CUI: C0020538
Disease:
Hypertensive disease
0.040 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: rs2070744
rs2070744
Entrez Id: 4846
Gene Symbol: NOS3
NOS3
CUI: C0020538
Disease:
Hypertensive disease
0.040 GeneticVariation BEFREE We therefore aimed to meta-analyze three eNOS widely-evaluated polymorphisms, G894T (rs1799983) in exon 7, 4b/a in intron 4, and T-786C (rs2070744) in promoter region, in association with hypertension from both English and Chinese publications, while addressing between-study heterogeneity and publication bias. 21912683 2011
dbSNP: rs2070744
rs2070744
Entrez Id: 4846
Gene Symbol: NOS3
NOS3
CUI: C0020538
Disease:
Hypertensive disease
0.040 GeneticVariation BEFREE To examine the relationship of three eNOS gene polymorphisms, T-786C (rs2070744), G894T (rs1799983), and G10T (rs7830), with hypertension in the Han population in southwestern China, we carried out a study of the genotypes of three SNPs in 510 hypertensive and 510 normotensive subjects from the Yunnan Province by using PCR-RFLP and sequencing. 21968727 2011