{{Rsnum
|rsid=12734991
|Gene=NOS1AP
|Chromosome=1
|position=162224786
|Orientation=plus
|GMAF=0.3466
|Gene_s=NOS1AP
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 20.4 | 47.8 | 31.9
| HCB | 59.6 | 32.4 | 8.1
| JPT | 39.8 | 44.2 | 15.9
| YRI | 94.6 | 5.4 | 0.0
| ASW | 71.9 | 26.3 | 1.8
| CHB | 59.6 | 32.4 | 8.1
| CHD | 53.7 | 40.7 | 5.6
| GIH | 51.5 | 35.6 | 12.9
| LWK | 93.6 | 6.4 | 0.0
| MEX | 22.8 | 45.6 | 31.6
| MKK | 59.6 | 39.1 | 1.3
| TSI | 25.5 | 44.1 | 30.4
| HapMapRevision=28
}}{{PMID Auto
|PMID=22682551
|Title=Common Variation in the NOS1AP Gene Is Associated With Drug-Induced QT Prolongation and Ventricular Arrhythmia
|OA=1
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}