{{Rsnum
|rsid=11708996
|Gene=SCN5A
|Chromosome=3
|position=38592432
|Orientation=plus
|GMAF=0.08999
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene_s=SCN5A
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;G)
| geno3=(G;G)
| CEU | 0.0 | 40.0 | 60.0
| HCB | 0.0 | 4.4 | 95.6
| JPT | 0.0 | 4.4 | 95.6
| YRI | 0.0 | 0.0 | 100.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 0.0 | 4.4 | 95.6
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20062060
|Trait=PR interval
|Title=Genome-wide association study of PR interval.
|RiskAllele=C
|Pval=6E-26
|OR=3.04
|ORtxt=[2.47-3.61] ms increase
|OA=1
}}

{{PMID Auto GWAS
|PMID=21076409
|Trait=None
|Title=Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction
|RiskAllele=C
|Pval=0.000007
|OR=0.4700
|ORtxt=[NR] ms increase
|OA=1
}}

{{PMID Auto
|PMID=21347284
|Title=Genome-wide association studies of the PR interval in African Americans.
|OA=1
}}

{{PMID Auto GWAS
  |PMID=23872634
  |Trait=Brugada syndrome
  |Title=Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death.
  |RiskAllele=C
  |Pval=1E-14
  |OR=1.73
  |ORtxt=[1.51-1.99]
  }}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}