{{Rsnum
|rsid = 28937317
|Gene = SCN5A
|geno1 = (A;A)
|geno2 = (A;G)
|geno3 = (G;G)
|Orientation=minus
|ReferenceAllele=A
|MissenseAllele=G
|Chromosome=3
|position=38560418
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=SCN5A
}}{{omim
|desc=LONG QT SYNDROME 3
|id=600163
|rsnum=28937317
|variant=0003
}}
{{ neighbor
| rsid = 28936971
| distance = 248
}}{{ClinVar
|rsid=28937317
|Reversed=1
|FwdREF=A
|FwdALT=G
|REF=T
|ALT=C
|RSPOS=38601909
|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.38601909T>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=600163.0003
|CLNSIG=5
|CLNCUI=C1859062
|CLNDBN=Long QT syndrome 3; not provided
|Disease=Long QT syndrome 3; not provided
|CLNACC=RCV000009964.1; RCV000058618.1
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1129:C1859062:603830:101016
}}{{PMID Auto
|PMID=8541846
|Title=Cardiac sodium channel mutations in patients with long QT syndrome, an inherited cardiac arrhythmia.
}}

{{PMID Auto
|PMID=10973849
|Title=Spectrum of mutations in long-QT syndrome genes. KVLQT1, HERG, SCN5A, KCNE1, and KCNE2.
}}

{{PMID Auto
|PMID=14736542
|Title=Mechanisms by which SCN5A mutation N1325S causes cardiac arrhythmias and sudden death in vivo.
|OA=1
}}

{{PMID Auto
|PMID=15840476
|Title=Compendium of cardiac channel mutations in 541 consecutive unrelated patients referred for long QT syndrome genetic testing.
}}

{{PMID Auto
|PMID=17905336
|Title=Long QT and Brugada syndrome gene mutations in New Zealand.
}}