{{Rsnum
|rsid=199473207
|Chromosome=3
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=SCN5A
|position=38566555
|Gene_s=SCN5A
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=199473207
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=38608046
|CHROM=3
|dbSNPBuildID=136
|SSR=0
|SAO=1
|VP=0x050168000000000002110100
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000003.11:g.38608046G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=600163.0004
|CLNSIG=5
|CLNCUI=CN029323
|CLNDBN=Brugada syndrome 1; not provided
|Disease=Brugada syndrome 1; not provided
|CLNACC=RCV000009965.1; RCV000058588.1
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1517:CN029323:601144:130:418818005
|GENEINFO=SCN5A:6331
|GENE_ID=6331
|GENE_NAME=SCN5A
}}{{PMID|9521325}} Genetic basis and molecular mechanism for idiopathic ventricular fibrillation.

{{PMID|19251209}} Type of SCN5A mutation determines clinical severity and degree of conduction slowing in loss-of-function sodium channelopathies.

{{PMID|20129283|OA=1
}} An international compendium of mutations in the SCN5A-encoded cardiac sodium channel in patients referred for Brugada syndrome genetic testing.

{{PMID|21321465}} Identification of six novel SCN5A mutations in Japanese patients with Brugada syndrome.