NOS3, nitric oxide synthase 3, 4846

N. diseases: 706; N. variants: 39
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1799983
rs1799983
Entrez Id: 4846
Gene Symbol: NOS3
NOS3
CUI: C0085580
Disease:
Essential Hypertension
0.100 GeneticVariation BEFREE The Glu298Asp polymorphism may contribute to the complex pathogenesis of essential hypertension and may be a factor in the resistance of these patients to conventional antihypertensive therapy. 11394896 2001
dbSNP: rs1799983
rs1799983
Entrez Id: 4846
Gene Symbol: NOS3
NOS3
CUI: C0085580
Disease:
Essential Hypertension
0.100 GeneticVariation BEFREE Given the evidence of positive association of another polymorphism in the eNOS gene, the Glu298Asp polymorphism, with essential hypertension, special attention will be required to interpret the results of a case-control study for genetic risk factors. 11131266 2000
dbSNP: rs1799983
rs1799983
Entrez Id: 4846
Gene Symbol: NOS3
NOS3
CUI: C0085580
Disease:
Essential Hypertension
0.100 GeneticVariation BEFREE Significant association between a Glu298Asp polymorphism of the endothelial nitric oxide synthase (eNOS) gene and essential hypertension was recently reported in Japanese populations, with the 298Asp variant showing a higher prevalence in hypertensive patients (10.3% to 12.0%) than in normotensive subjects (5.0% to 5.8%). 10205226 1999
dbSNP: rs1799983
rs1799983
Entrez Id: 4846
Gene Symbol: NOS3
NOS3
CUI: C0085580
Disease:
Essential Hypertension
0.100 GeneticVariation BEFREE In conclusion, the Glu298Asp missense variant was significantly associated with essential hypertension, which suggests that it is a genetic susceptibility factor for essential hypertension. 9674630 1998