{{Rsnum
|rsid=137854606
|Chromosome=3
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=SCN5A
|position=38604062
|Gene_s=SCN5A
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=600163
|variant=0016
|rsnum=137854606
}}{{ClinVar
|rsid=137854606
|Reversed=1
|FwdREF=G
|FwdALT=T
|REF=C
|ALT=A
|RSPOS=38645553
|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.38645553C>A
|CLNORIGIN=1
|CLNSIG=5
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|CLNACC=RCV000009984.1; RCV000058427.1
|CLNDBN=Cardiac conduction defect, nonprogressive; not provided
|CLNDSDB=MedGen
|CLNDSDBID=C1861984
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=600163.0016
|Disease=Cardiac conduction defect; not provided
}}{{PMID Auto
|PMID=11234013
|Title=A sodium-channel mutation causes isolated cardiac conduction disease.
}}

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