{{Rsnum
|rsid=1808593
|Chromosome=7
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=NOS3
|position=151011214
|Gene_s=NOS3
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 1.7 | 30.0 | 68.3
| HCB | 0.0 | 26.3 | 73.7
| JPT | 7.7 | 25.6 | 66.7
| YRI | 5.5 | 40.0 | 54.5
| ASW | 0.0 | 0.0 | 0.0
| CHB | 0.0 | 26.3 | 73.7
| 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=25140814
|Title=Association of NOS3 gene variants and clinical contributors of hypoxic-ischemic encephalopathy
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}