{{Rsnum
|rsid=397514449
|Chromosome=3
|Orientation=minus
|geno1=(-;-)
|geno2=(-;TGA)
|geno3=(TGA;TGA)
|Gene=SCN5A
|position=38550984
|Gene_s=SCN5A
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=CTCA
|CHROM=3
|CLNACC=RCV000009979.2; RCV000009980.2
|CLNALLE=1
|CLNDBN=Long QT syndrome 3; Brugada syndrome 1
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet; GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1129:C1859062:603830:101016; NBK1517:CN029323:601144:130:418818005
|CLNHGVS=NC_000003.11:g.38592476_38592478dupTCA
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=600163.0013
|Disease=Long QT syndrome 3; Brugada syndrome 1
|FwdALT=TGA
|GENEINFO=SCN5A:6331
|GENE_ID=6331
|GENE_NAME=SCN5A
|REF=C
|RSPOS=38592475
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050060000000000002110200
|WGT=0
|dbSNPBuildID=136
|rsid=397514449
}}