{{Rsnum
|rsid=137854618
|Chromosome=3
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=SCN5A
|position=38566426
|Gene_s=SCN5A
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=600163
|variant=0034
|rsnum=137854618
}}{{ClinVar
|rsid=137854618
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=38607917
|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.38607917C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=600163.0034
|CLNSIG=5
|CLNCUI=C1832680; C1838539; C3151464
|CLNDBN=Dilated cardiomyopathy 1E; Atrial standstill; Atrial fibrillation, familial, 10; not provided
|Disease=Dilated cardiomyopathy 1E; Atrial standstill; Atrial fibrillation; not provided
|CLNACC=RCV000010003.1; RCV000010004.1; RCV000022946.1; RCV000058604.1
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet; MedGen:OMIM:Orphanet; MedGen:OMIM
|CLNDSDBID=NBK1309:C1832680:601154:154; C1838539:108770:1344; C3151464:614022
}}{{PMID Auto
|PMID=20384
|Title=An enzymatic time/temperature device for monitoring the handling of perishable commodities.
}}

{{PMID Auto
|PMID=12522116
|Title=A cardiac sodium channel mutation cosegregates with a rare connexin40 genotype in familial atrial standstill.
}}

{{PMID Auto
|PMID=15466643
|Title=SCN5A mutation associated with dilated cardiomyopathy, conduction disorder, and arrhythmia.
}}

{{PMID Auto
|PMID=16684018
|Title=SCN5A mutation associated with cardiac conduction defect and atrial arrhythmias.
}}

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

{{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
}}