{{Rsnum
|rsid=121434386
|Chromosome=11
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=SCN4B
|position=118141265
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=SCN4B
}}{{omim
|id=608256
|rsnum=121434386
|variant=0001
}}{{ClinVar
|rsid=121434386
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=118011980
|CHROM=11
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=SCN4B:6330
|GENE_NAME=SCN4B
|GENE_ID=6330
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.118011980G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=608256.0001
|CLNSIG=5
|CLNCUI=C2678484
|CLNDBN=Long QT syndrome 10
|Disease=Long QT syndrome 10
|CLNACC=RCV000002563.1
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1129:C2678484:611819:101016
}}