{{Rsnum
|rsid = 28937318
|Gene = SCN5A
|geno1 = (A;A)
|geno2 = (A;G)
|geno3 = (G;G)
|Orientation=minus
|ReferenceAllele=G
|MissenseAllele=A
|Chromosome=3
|position=38606709
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=SCN5A
}}{{omim
|desc=BRUGADA SYNDROME
|id=600163
|rsnum=28937318
|variant=0021
}}

{{ClinVar
|rsid=28937318
|Reversed=1
|FwdREF=G
|FwdALT=A,T
|REF=C
|ALT=A,T
|RSPOS=38648200
|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; 2
|CLNHGVS=NC_000003.11:g.38648200C>A; NC_000003.11:g.38648200C>T
|CLNORIGIN=1
|CLNSRCID=
600163.0021
|CLNSIG=5
|CLNCUI=
|CLNACC=
RCV000058391.1; RCV000009988.2; RCV000058390.1
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDBN=not provided; Brugada syndrome 1
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1517:CN029323:601144:130:418818005
|CLNSRC=OMIM Allelic Variant
|Disease=not provided; Brugada syndrome 1
}}

{{PMID Auto
|PMID=19214780
|Title=In silico investigations on functional and haplotype tag SNPs associated with congenital long QT syndromes (LQTSs).
|OA=1
}}

{{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=11823453
|Title=Genetic and biophysical basis of sudden unexplained nocturnal death syndrome (SUNDS), a disease allelic to Brugada syndrome.
}}

{{PMID Auto
|PMID=14687250
|Title=A cardiac sodium channel mutation identified in Brugada syndrome associated with atrial standstill.
}}

{{PMID Auto
|PMID=15028074
|Title=Phenotypic characterization of a large European family with Brugada syndrome displaying a sudden unexpected death syndrome mutation in SCN5A:.
}}

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

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}