{{Rsnum
|rsid=1805126
|Gene=SCN5A
|Chromosome=3
|position=38550915
|Orientation=minus
|GMAF=0.4936
|Gene_s=SCN5A
|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 | 11.5 | 40.7 | 47.8
| HCB | 27.0 | 53.3 | 19.7
| JPT | 23.0 | 56.6 | 20.4
| YRI | 55.8 | 36.1 | 8.2
| ASW | 31.6 | 54.4 | 14.0
| CHB | 27.0 | 53.3 | 19.7
| CHD | 31.2 | 46.8 | 22.0
| GIH | 12.9 | 34.7 | 52.5
| LWK | 59.1 | 38.2 | 2.7
| MEX | 19.0 | 55.2 | 25.9
| MKK | 57.1 | 38.5 | 4.5
| TSI | 13.7 | 45.1 | 41.2
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23463857
  |Trait=Electrocardiographic conduction measures
  |Title=Genome- and phenome-wide analyses of cardiac conduction identifies markers of arrhythmia risk.
  |RiskAllele=A
  |Pval=3E-20
  |OR=.66
  |ORtxt=[NR] msec decrease
  |OA=1
}}

{{PMID Auto
|PMID=17534376
|Title=Confirmation of associations between ion channel gene SNPs and QTc interval duration in healthy subjects.
|OA=1
}}

{{PMID Auto
|PMID=18368697
|Title=SCN5A variants in Japanese patients with left ventricular noncompaction and arrhythmia.
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}