{{Rsnum
|rsid=199473282
|Chromosome=3
|Orientation=minus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=SCN5A
|position=38551513
|Gene_s=SCN5A
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=199473282
|Reversed=1
|FwdREF=C
|FwdALT=A,T
|REF=G
|ALT=A,T
|RSPOS=38593004
|CHROM=3
|dbSNPBuildID=136
|SSR=0
|SAO=1
|VP=0x050168000000000002110100
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000003.11:g.38593004G>A; NC_000003.11:g.38593004G>T
|CLNORIGIN=1
|CLNSRCID=
600163.0004
|CLNSIG=5
|CLNCUI=
|CLNACC=
RCV000009965.1; RCV000058715.1; RCV000058714.1
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDBN=Brugada syndrome 1; not provided
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1517:CN029323:601144:130:418818005
|CLNSRC=OMIM Allelic Variant
|Disease=Brugada syndrome 1; not provided
|GENEINFO=SCN5A:6331
|GENE_ID=6331
|GENE_NAME=SCN5A
}}{{PMID Auto
|PMID=18065446
|Title=Combination of cardiac conduction disease and long QT syndrome caused by mutation T1620K in the cardiac sodium channel.
}}

{{PMID Auto
|PMID=21552533
|Title=Alternative splicing of the cardiac sodium channel creates multiple variants of mutant T1620K channels.
|OA=1
}}

{{PMID Auto
|PMID=9521325
|Title=Genetic basis and molecular mechanism for idiopathic ventricular fibrillation.
}}

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