{{Rsnum
|rsid = 28937316
|Gene = SCN5A
|geno1 = (A;A)
|geno2 = (A;G)
|geno3 = (G;G)
|Orientation=minus
|ReferenceAllele=G
|MissenseAllele=A
|Chromosome=3
|position=38551441
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=SCN5A
}}{{omim
|desc=LONG QT SYNDROME 3
|id=600163
|rsnum=28937316
|variant=0002
}}

{{ClinVar
|rsid=28937316
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=38592932
|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.38592932C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=600163.0002
|CLNSIG=5
|CLNCUI=C1859062
|CLNDBN=Long QT syndrome 3; not provided
|Disease=Long QT syndrome 3; not provided
|CLNACC=RCV000009963.3; RCV000058726.1
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1129:C1859062:603830:101016
}}

{{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=862061
|Title=[Machanisms in the prenatal development of the ovary].
}}

{{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=15051636
|Title=Compound mutations: a common cause of severe long-QT syndrome.
}}

{{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=19841300
|Title=Genetic testing for long-QT syndrome: distinguishing pathogenic mutations from benign variants.
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}