{{Rsnum
|rsid=3922844
|Gene=SCN5A
|Chromosome=3
|position=38582762
|Orientation=minus
|GMAF=0.3375
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=SCN5A
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 7.1 | 39.8 | 53.1
| HCB | 1.5 | 23.4 | 75.2
| JPT | 2.7 | 31.0 | 66.4
| YRI | 46.3 | 43.5 | 10.2
| ASW | 31.6 | 52.6 | 15.8
| CHB | 1.5 | 23.4 | 75.2
| CHD | 0.0 | 17.4 | 82.6
| GIH | 2.0 | 43.6 | 54.5
| LWK | 45.0 | 41.3 | 13.8
| MEX | 5.2 | 27.6 | 67.2
| MKK | 41.0 | 44.2 | 14.7
| TSI | 13.7 | 38.2 | 48.0
| HapMapRevision=28
}}{{PMID Auto
|PMID=21347284
|Title=Genome-Wide Association Studies of the PR Interval in African Americans
|OA=1
}}

{{PMID Auto GWAS
  |PMID=23139255
  |Trait=PR interval
  |Title=Novel Loci Associated With PR Interval in a Genome-Wide Association Study of 10 African American Cohorts.
  |RiskAllele=T
  |Pval=5E-43
  |OR=4.54
  |ORtxt=[3.89-5.19] unit decrease
  |OA=1
}}

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