{{Rsnum
|rsid=137854607
|Chromosome=3
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=SCN5A
|position=38554309
|Gene_s=SCN5A
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=600163
|variant=0017
|rsnum=137854607
}}
{{omim
|id=600163
|variant=0039
|rsnum=137854607
}}{{ClinVar
|rsid=137854607
|Reversed=1
|FwdREF=G
|FwdALT=A,C
|REF=C
|ALT=G,T
|RSPOS=38595800
|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.38595800C>G; NC_000003.11:g.38595800C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=600163.0039; 600163.0017
|CLNSIG=5
|CLNCUI=C1832680; C1879286
|CLNDBN=Dilated cardiomyopathy 1E; not provided; Progressive familial heart block type 1A
|Disease=Dilated cardiomyopathy 1E; not provided; Progressive familial heart block type 1A
|CLNACC=RCV000010009.1; RCV000058706.1; RCV000009983.1; RCV000058705.1
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet; MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1309:C1832680:601154:154; C1879286:113900:871
}}{{PMID Auto
|PMID=15671429
|Title=Sodium channel mutations and susceptibility to heart failure and atrial fibrillation.
|OA=1
}}

{{PMID Auto
|PMID=18048769
|Title=Divergent biophysical defects caused by mutant sodium channels in dilated cardiomyopathy with arrhythmia.
}}

{{PMID Auto
|PMID=11804990
|Title=Clinical, genetic, and biophysical characterization of SCN5A mutations associated with atrioventricular conduction block.
}}