{{Rsnum
|rsid=137854608
|Chromosome=3
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=SCN5A
|position=38609776
|Gene_s=SCN5A
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=600163
|variant=0018
|rsnum=137854608
}}{{ClinVar
|rsid=137854608
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=38651267
|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.38651267C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=600163.0018
|CLNSIG=5
|CLNCUI=C1879286
|CLNDBN=Progressive familial heart block type 1A; not provided
|Disease=Progressive familial heart block type 1A; not provided
|CLNACC=RCV000009985.1; RCV000058858.1
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1879286:113900:871
}}{{PMID Auto
|PMID=11804990
|Title=Clinical, genetic, and biophysical characterization of SCN5A mutations associated with atrioventricular conduction block.
}}

{{PMID Auto
|PMID=19056759
|Title=Sodium channel mutation in irritable bowel syndrome: evidence for an ion channelopathy.
|OA=1
}}