{{Rsnum
|rsid=45620037
|Gene=SCN5A
|Chromosome=3
|position=38613787
|Orientation=minus
|GMAF=0.0004591
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=SCN5A
}}{{omim
|id=600163
|rsnum=45620037
|variant=0027
}}
{{omim
|id=600163
|rsnum=45620037
|variant=0037
}}

{{ClinVar
|rsid=45620037
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=38655278
|CHROM=3
|GMAF=0.0005
|dbSNPBuildID=127
|SSR=0
|SAO=1
|VP=0x050168000000000116110100
|GENEINFO=SCN5A:6331
|GENE_NAME=SCN5A
|GENE_ID=6331
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000003.11:g.38655278G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=600163.0027; 600163.0037
|CLNSIG=5
|CLNCUI=C1837845
|CLNDBN=Sick sinus syndrome 1, autosomal recessive; Dilated cardiomyopathy 1E; not provided
|Disease=Sick sinus syndrome 1; Dilated cardiomyopathy 1E; not provided
|CLNACC=RCV000009998.1; RCV000030889.1; RCV000058832.1
|Tags=RV;PM;PMC;SLO;GNO;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9995; 0.0004591
|CLNDSDB=MedGen:OMIM:Orphanet; GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=C1837845:608567:166282; NBK1309:C1832680:601154:154
|COMMON=0
}}

{{PMID|19214780|OA=1
}} In silico investigations on functional and haplotype tag SNPs associated with congenital long QT syndromes (LQTSs).

{{PMID|14523039|OA=1
}} Congenital sick sinus syndrome caused by recessive mutations in the cardiac sodium channel gene (SCN5A).

{{PMID|15671429|OA=1
}} Sodium channel mutations and susceptibility to heart failure and atrial fibrillation.

{{PMID|20129283|OA=1
}} An international compendium of mutations in the SCN5A-encoded cardiac sodium channel in patients referred for Brugada syndrome genetic testing.

{{PMID|20448214|OA=1
}} Mechanistic links between Na+ channel (SCN5A) mutations and impaired cardiac pacemaking in sick sinus syndrome.

{{PMID|20539757|OA=1
}} Multiple loss-of-function mechanisms contribute to SCN5A-related familial sick sinus syndrome.

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