{{Rsnum
|rsid=137854617
|Chromosome=3
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=SCN5A
|position=38581002
|Gene_s=SCN5A
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=600163
|variant=0033
|rsnum=137854617
}}{{ClinVar
|rsid=137854617
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=38622493
|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.38622493C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=600163.0033
|CLNSIG=5
|CLNCUI=CN029323; C3151464
|CLNDBN=Brugada syndrome 1; Atrial fibrillation, familial, 10; not provided
|Disease=Brugada syndrome 1; Atrial fibrillation; not provided
|CLNACC=RCV000010002.1; RCV000022945.1; RCV000058552.1
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT; MedGen:OMIM
|CLNDSDBID=NBK1517:CN029323:601144:130:418818005; C3151464:614022
}}{{PMID Auto
|PMID=11076825
|Title=Clinical and genetic heterogeneity of right bundle branch block and ST-segment elevation syndrome: A prospective evaluation of 52 families.
}}

{{PMID Auto
|PMID=11901046
|Title=Natural history of Brugada syndrome: insights for risk stratification and management.
}}

{{PMID Auto
|PMID=19716085
|Title=Spectrum and prevalence of mutations from the first 2,500 consecutive unrelated patients referred for the FAMILION long QT syndrome genetic test.
|OA=1
}}