{{Rsnum
|rsid=41313031
|Gene=SCN5A
|Chromosome=3
|position=38562456
|Orientation=plus
|GMAF=0.002755
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=SCN5A
}}{{omim
|id=600163
|rsnum=41313031
|variant=0040
}}{{ClinVar
|rsid=41313031
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=38603947
|CHROM=3
|GMAF=0.0027
|dbSNPBuildID=127
|SSR=0
|SAO=1
|VP=0x050178000000000116110100
|GENEINFO=SCN5A:6331
|GENE_NAME=SCN5A
|GENE_ID=6331
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000003.11:g.38603947G>A
|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; RCV000058614.1
|Tags=PM;TPA;PMC;SLO;GNO;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9972; 0.002755
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1517:CN029323:601144:130:418818005
|COMMON=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=15851227
|Title=Spectrum and prevalence of cardiac sodium channel variants among black, white, Asian, and Hispanic individuals: implications for arrhythmogenic susceptibility and Brugada/long QT syndrome genetic testing.
}}

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

{{PMID Auto
|PMID=19841300
|Title=Genetic testing for long-QT syndrome: distinguishing pathogenic mutations from benign variants.
|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
}}