{{Rsnum
|rsid=137854601
|Chromosome=3
|position=38551022
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=SCN5A
|Gene_s=SCN5A
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=600163
|variant=0008
|rsnum=137854601
}}{{ClinVar
|rsid=137854601
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=38592513
|CHROM=3
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050368000000000002110100
|GENEINFO=SCN5A:6331
|GENE_NAME=SCN5A
|GENE_ID=6331
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000003.11:g.38592513C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=600163.0008
|CLNSIG=5
|CLNCUI=C1859062; CN029323
|CLNDBN=Long QT syndrome 3; Brugada syndrome 1; Sinus node disease; not provided
|Disease=Long QT syndrome 3; Brugada syndrome 1; Sinus node disease; not provided
|CLNACC=RCV000009972.1; RCV000009973.1; RCV000009974.1; RCV000058773.1
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet; GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT; MedGen
|CLNDSDBID=NBK1129:C1859062:603830:101016; NBK1517:CN029323:601144:130:418818005; C0428908
}}{{PMID Auto
|PMID=15840
|Title=The purification and properties of NADP-dependent isocitrate dehydrogenase from ox-heart mitochondria.
}}

{{PMID Auto
|PMID=10377081
|Title=Congenital long-QT syndrome caused by a novel mutation in a conserved acidic domain of the cardiac Na+ channel.
}}

{{PMID Auto
|PMID=10961955
|Title=The elusive link between LQT3 and Brugada syndrome: the role of flecainide challenge.
}}

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

{{PMID Auto
|PMID=11901046
|Title=Natural history of Brugada syndrome: insights for risk stratification and management.
}}

{{PMID Auto
|PMID=12877697
|Title=Catecholamine-provoked microvoltage T wave alternans in genotyped long QT syndrome.
}}