{{Rsnum
|rsid=137854603
|Chromosome=3
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=SCN5A
|position=38550602
|Gene_s=SCN5A
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=600163
|variant=0012
|rsnum=137854603
}}{{ClinVar
|rsid=137854603
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=38592093
|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.38592093C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=600163.0012
|CLNSIG=5
|CLNCUI=CN029323
|CLNDBN=Brugada syndrome 1; not provided
|Disease=Brugada syndrome 1; not provided
|CLNACC=RCV000009978.1; RCV000058806.1
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1517:CN029323:601144:130:418818005
}}{{PMID Auto
|PMID=10690282
|Title=Human SCN5A gene mutations alter cardiac sodium channel kinetics and are associated with the Brugada syndrome.
}}

{{PMID Auto
|PMID=12106943
|Title=Genotype-phenotype relationship in Brugada syndrome: electrocardiographic features differentiate SCN5A-related patients from non-SCN5A-related patients.
}}

{{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
}}