{{Rsnum
|rsid=1800783
|Gene=NOS3
|Chromosome=7
|position=150992309
|Orientation=plus
|GMAF=0.332
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene_s=NOS3
}}Note: this SNP should perhaps be best seen as a proxy for [[rs4496877]], a SNP assayed by the Illumina 1M chip. The pairwise r(2) linkage between the two is reported to be 0.96.{{PMID|20962522}}

{{ population diversity
| geno1=(A;A)
| geno2=(A;T)
| geno3=(T;T)
| CEU | 15.4 | 50.8 | 33.8
| HCB | 0.0 | 24.4 | 75.6
| JPT | 0.0 | 11.4 | 88.6
| YRI | 15.9 | 54.0 | 30.2
| ASW | 0.0 | 0.0 | 0.0
| CHB | 0.0 | 24.4 | 75.6
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{PMID Auto
|PMID=19853644
|Title=Promoter polymorphisms of the NOS3 gene are associated with hypnotizability-dependent vascular response to nociceptive stimulation
}}
{{PMID Auto
|PMID=20409549
|Title=NOS3 gene polymorphisms are associated with risk markers of cardiovascular disease, and interact with omega-3 polyunsaturated fatty acids
}}
{{PMID Auto
|PMID=20962522
|Title=Genetic Polymorphisms in Nitric Oxide Synthase 3 Gene and Implications for Kidney Disease: A Meta-Analysis
}}

{{PMID Auto
|PMID=17980690
|Title=Polymorphisms in the endothelial nitric oxide synthase gene and bone density/ultrasound and geometry in humans.
|OA=1
}}

{{PMID Auto
|PMID=18246059
|Title=Habitual energy expenditure modifies the association between NOS3 gene polymorphisms and blood pressure.
|OA=1
}}

{{PMID Auto
|PMID=18663495
|Title=Nitric oxide synthase genes and their interactions with environmental factors in Parkinson's disease.
|OA=1
}}

{{PMID Auto
|PMID=21252862
|Title=NOS3 variants, physical activity, and blood pressure in the European Youth Heart Study.
}}

{{PMID Auto
|PMID=21674837
|Title=Association of NOS3 tag polymorphisms with hypoxic-ischemic encephalopathy.
|OA=1
}}

{{PMID Auto
|PMID=23021696
|Title=Single-nucleotide polymorphisms in genes involved in placental function and unexplained stillbirth
}}

{{PMID Auto
|PMID=24035903
|Title=The -974 C&gt;A (rs3087459) gene polymorphism in the endothelin gene (EDN1) is associated with risk of developing acute coronary syndrome in Mexican patients
}}

{{PMID Auto
|PMID=23826716
|Title=Association analysis of nitric oxide synthases: NOS1, NOS2A and NOS3 genes, with multiple sclerosis.
}}

{{PMID Auto
|PMID=25140814
|Title=Association of NOS3 gene variants and clinical contributors of hypoxic-ischemic encephalopathy
}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}