{{Rsnum
|rsid=137854609
|Chromosome=3
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=SCN5A
|position=38581170
|Gene_s=SCN5A
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=600163
|variant=0019
|rsnum=137854609
}}{{ClinVar
|rsid=137854609
|Reversed=1
|FwdREF=G
|FwdALT=A,T
|REF=C
|ALT=A,T
|RSPOS=38622661
|CHROM=3
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050168000000000002110100
|GENEINFO=SCN5A:6331
|GENE_NAME=SCN5A
|GENE_ID=6331
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000003.11:g.38622661C>A; NC_000003.11:g.38622661C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=600163.0019
|CLNSIG=5
|CLNCUI=C1859062
|CLNDBN=Long QT syndrome 3; not provided
|Disease=Long QT syndrome 3; not provided
|CLNACC=RCV000009986.1; RCV000058542.1; RCV000058541.1
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1129:C1859062:603830:101016
}}{{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
}}

{{PMID Auto
|PMID=11710892
|Title=Postmortem molecular analysis of SCN5A defects in sudden infant death syndrome.
}}

{{PMID Auto
|PMID=19716085
|Title=Spectrum and prevalence of mutations from the first 2,500 consecutive unrelated patients referred for the FAMILION long QT syndrome genetic test.
|OA=1
}}