{{Rsnum
|rsid=10918859
|Gene=NOS1AP
|Chromosome=1
|position=162199478
|Orientation=plus
|GMAF=0.2103
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=NOS1AP
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 2.7 | 29.2 | 68.1
| HCB | 10.2 | 43.1 | 46.7
| JPT | 15.0 | 44.2 | 40.7
| YRI | 0.0 | 0.0 | 100.0
| ASW | 0.0 | 8.8 | 91.2
| CHB | 10.2 | 43.1 | 46.7
| CHD | 9.3 | 51.9 | 38.9
| GIH | 14.9 | 47.5 | 37.6
| LWK | 0.0 | 0.0 | 0.0
| MEX | 1.7 | 31.0 | 67.2
| MKK | 0.0 | 0.6 | 99.4
| TSI | 6.9 | 41.2 | 52.0
| HapMapRevision=28
}}{{PMID Auto
|PMID=21685173
|Title=Common Variants in CASQ2, GPD1L and NOS1AP Are Significantly Associated with Risk of Sudden Death in Patients with Coronary Artery Disease
|OA=1
}}

{{PMID Auto
|PMID=23171141
|Title=Positive association between rs10918859 of the NOS1AP gene and coronary heart disease in male Han Chinese.
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | Illumina Human 1M}}