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: C0151744
Disease:
Myocardial Ischemia
0.030 GeneticVariation BEFREE The GluAsp or AspAsp genotype of the Glu298Asp polymorphism was significantly associated with IHD, but not albuminuria in these Japanese diabetic subjects. 18243394 2008
dbSNP: rs1799983
rs1799983
Entrez Id: 4846
Gene Symbol: NOS3
NOS3
CUI: C0151744
Disease:
Myocardial Ischemia
0.030 GeneticVariation BEFREE Using robust family-based association tests specifically designed for the study of complex diseases, we found no evidence that the G894T polymorphism of the eNOS gene has a significant role in the development of IHD in our population. 15523316 2004
dbSNP: rs1799983
rs1799983
Entrez Id: 4846
Gene Symbol: NOS3
NOS3
CUI: C0151744
Disease:
Myocardial Ischemia
0.030 GeneticVariation BEFREE In this context, a genetic association study was carried out between two eNOS polymorphisms (the ecNOS4a/b VNTR and the G894T substitution) in a sample of 101 nuclear families having one affected offspring of ischemic heart disease (IHD). 12503100 2003