{{Rsnum
|rsid=137854604
|Chromosome=3
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=SCN5A
|position=38551243
|Gene_s=SCN5A
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=600163
|variant=0014
|rsnum=137854604
}}{{ClinVar
|rsid=137854604
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=38592734
|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
|CLNHGVS=NC_000003.11:g.38592734G>A
|CLNORIGIN=1
|CLNSIG=5
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|CLNACC=RCV000009981.1; RCV000058743.1
|CLNDBN=Ventricular fibrillation, paroxysmal familial; not provided
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=600163.0014
|Disease=Ventricular fibrillation; not provided
}}{{PMID Auto
|PMID=10940383
|Title=A novel SCN5A mutation associated with idiopathic ventricular fibrillation without typical ECG findings of Brugada syndrome.
}}

{{PMID Auto
|PMID=11827685
|Title=A mutant cardiac sodium channel with multiple biophysical defects associated with overlapping clinical features of Brugada syndrome and cardiac conduction disease.
}}

{{PMID Auto
|PMID=17141278
|Title=A novel mutation in the SCN5A gene is associated with Brugada syndrome.
}}