{{Rsnum
|rsid=137854619
|Chromosome=3
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=SCN5A
|position=38550917
|Gene_s=SCN5A
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=600163
|variant=0035
|rsnum=137854619
}}{{ClinVar
|rsid=137854619
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=38592408
|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.38592408C>T
|CLNORIGIN=1
|CLNSIG=5
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNACC=RCV000010005.1; RCV000058782.1
|CLNDBN=Long QT syndrome 2/3, digenic; not provided
|CLNDSDB=MedGen
|CLNDSDBID=C3276240
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=600163.0035
|Disease=Long QT syndrome 2/3; not provided
}}{{PMID Auto
|PMID=16922724
|Title=Spectrum of pathogenic mutations and associated polymorphisms in a cohort of 44 unrelated patients with long QT syndrome.
}}