{{Rsnum
|rsid=1415259
|Gene=NOS1AP
|Chromosome=1
|position=162115519
|Orientation=minus
|GMAF=0.4775
|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 | 40.7 | 48.7 | 10.6
| HCB | 14.1 | 37.8 | 48.1
| JPT | 10.0 | 41.8 | 48.2
| YRI | 7.5 | 45.9 | 46.6
| ASW | 12.3 | 47.4 | 40.4
| CHB | 14.1 | 37.8 | 48.1
| CHD | 10.1 | 45.0 | 45.0
| GIH | 9.0 | 33.0 | 58.0
| LWK | 9.3 | 28.7 | 62.0
| MEX | 43.1 | 39.7 | 17.2
| MKK | 16.8 | 47.1 | 36.1
| TSI | 45.1 | 45.1 | 9.8
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20062061
|Trait=Electrocardiographic traits
|Title=Genetic variation in SCN10A influences cardiac conduction
|RiskAllele=A
|Pval=7E-10
|OR=2.53
|ORtxt=[1.73-3.33] ms decrease
}}

{{PMID Auto
|PMID=20031603
|Title=A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project.
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | Illumina Human 1M}}