{{Rsnum
|rsid=45471994
|Chromosome=3
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=SCN5A
|position=38613752
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=SCN5A
}}{{omim
|id=600163
|rsnum=45471994
|variant=0040
}}

{{ClinVar
|rsid=45471994
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=38655243
|CHROM=3
|dbSNPBuildID=127
|SSR=0
|SAO=1
|VP=0x050168000000000502110100
|GENEINFO=SCN5A:6331
|GENE_NAME=SCN5A
|GENE_ID=6331
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000003.11:g.38655243C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=600163.0040
|CLNSIG=5
|CLNCUI=CN029323; CN029323
|CLNDBN=Brugada syndrome 1; not provided
|Disease=Brugada syndrome 1; not provided
|CLNACC=RCV000010010.2; RCV000058840.1
|Tags=RV;PM;PMC;SLO;HD;GNO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1517:CN029323:601144:130:418818005
}}

{{PMID|18599870|OA=1
}} Lidocaine-induced Brugada syndrome phenotype linked to a novel double mutation in the cardiac sodium channel.

{{PMID|20129283|OA=1
}} An international compendium of mutations in the SCN5A-encoded cardiac sodium channel in patients referred for Brugada syndrome genetic testing.

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}