{{Rsnum
|rsid=12742393
|Gene=NOS1AP
|Chromosome=1
|position=162254796
|Orientation=plus
|GMAF=0.3737
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene_s=NOS1AP
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 17.7 | 44.2 | 38.1
| HCB | 63.5 | 28.5 | 8.0
| JPT | 44.2 | 43.4 | 12.4
| YRI | 70.7 | 28.6 | 0.7
| ASW | 52.6 | 40.4 | 7.0
| CHB | 63.5 | 28.5 | 8.0
| CHD | 58.7 | 39.4 | 1.8
| GIH | 46.5 | 42.6 | 10.9
| LWK | 61.8 | 36.4 | 1.8
| MEX | 27.6 | 41.4 | 31.0
| MKK | 40.4 | 48.7 | 10.9
| TSI | 28.4 | 48.0 | 23.5
| HapMapRevision=28
}}{{PMID|19255043|OA=1
}} possible [[schizophrenia]] risk factor - A allele enhanced transcription factor binding and gene expression of NOS1AP (nitric oxide synthase 1 adaptor protein)

{{omim
|id=181500
|rsnum=12742393
}}

{{PMID Auto
|PMID=19937226
|Title=Association of genetic variants of NOS1AP with type 2 diabetes in a Chinese population.
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}