{{Rsnum
|rsid=45546039
|Chromosome=3
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=SCN5A
|position=38613781
|Gene_s=SCN5A
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=3
|CLNACC=RCV000032639.1; RCV000041637.1; RCV000058833.1
|CLNALLE=1
|CLNDBN=Dilated cardiomyopathy 1E; Primary dilated cardiomyopathy; not provided
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet; GeneReviews:MedGen:OMIM:SNOMED_CT
|CLNDSDBID=NBK1309:C1832680:601154:154; NBK1309:C0007193:212110:195021004
|CLNHGVS=NC_000003.11:g.38655272C>T
|CLNORIGIN=1
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=600163.0046
|Disease=Dilated cardiomyopathy 1E; Primary dilated cardiomyopathy; not provided
|FwdALT=A
|FwdREF=G
|GENEINFO=SCN5A:6331
|GENE_ID=6331
|GENE_NAME=SCN5A
|REF=C
|RSPOS=38655272
|Reversed=1
|SAO=1
|SSR=0
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD
|VC=SNV
|VP=0x050168000000000002100100
|WGT=0
|dbSNPBuildID=127
|rsid=45546039
}}

{{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=19412328
|Title=Coding sequence mutations identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 patients with familial or idiopathic dilated cardiomyopathy.
|OA=1
}}

{{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
}}

{{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
}}

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