{{Rsnum
|rsid=8068149
|Gene=NOS2
|Chromosome=17
|position=27761829
|Orientation=plus
|GMAF=0.4596
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=NOS2
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 12.7 | 50.9 | 36.4
| HCB | 44.4 | 44.4 | 11.3
| JPT | 49.1 | 42.7 | 8.2
| YRI | 42.7 | 44.1 | 13.3
| ASW | 42.1 | 40.4 | 17.5
| CHB | 44.4 | 44.4 | 11.3
| CHD | 41.7 | 50.0 | 8.3
| GIH | 47.0 | 41.0 | 12.0
| LWK | 31.5 | 55.6 | 13.0
| MEX | 17.2 | 41.4 | 41.4
| MKK | 51.3 | 43.6 | 5.1
| TSI | 23.5 | 44.1 | 32.4
| HapMapRevision=28
}}
{{PMID Auto
|PMID=18563708
|Title=Family-based association study between NOS-I and -IIA polymorphisms and autism spectrum disorders in Korean trios.
}}

{{PMID Auto
|PMID=19309520
|Title=Nitric oxide synthase 2A (NOS2A) polymorphisms are not associated with invasive pneumococcal disease.
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}