{{Rsnum
|rsid=137854612
|Chromosome=3
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=SCN5A
|position=38560170
|Gene_s=SCN5A
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=600163
|variant=0026
|rsnum=137854612
}}{{ClinVar
|rsid=137854612
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=38601661
|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.38601661C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=600163.0026
|CLNSIG=5
|CLNCUI=C1837845; CN029323
|CLNDBN=Sick sinus syndrome 1, autosomal recessive; Brugada syndrome 1; Cardiac conduction defect, nonspecific; not provided
|Disease=Sick sinus syndrome 1; Brugada syndrome 1; Cardiac conduction defect; not provided
|CLNACC=RCV000009995.1; RCV000009996.1; RCV000009997.1; RCV000058649.1
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet; GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT; MedGen
|CLNDSDBID=C1837845:608567:166282; NBK1517:CN029323:601144:130:418818005; C2748542
}}{{PMID Auto
|PMID=11748104
|Title=Novel SCN5A mutation leading either to isolated cardiac conduction defect or Brugada syndrome in a large French family.
}}

{{PMID Auto
|PMID=14523039
|Title=Congenital sick sinus syndrome caused by recessive mutations in the cardiac sodium channel gene (SCN5A).
|OA=1
}}

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

{{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=20539757
|Title=Multiple loss-of-function mechanisms contribute to SCN5A-related familial sick sinus syndrome.
|OA=1
}}