{{Rsnum
|rsid=199472721
|Chromosome=11
|position=2572848
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=KCNQ1
|Gene_s=KCNQ1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Orientation=plus
}}{{ClinVar
|ALT=C
|CHROM=11
|CLNACC=RCV000046127.2; RCV000057760.1
|CLNALLE=1
|CLNDBN=KCNQ1-related Jervell and Lange-Nielsen syndrome; not provided
|CLNDSDB=MedGen
|CLNDSDBID=CN177652
|CLNHGVS=NC_000011.9:g.2594078G>C
|CLNORIGIN=1
|CLNSIG=1
|Disease=KCNQ1-related Jervell and Lange-Nielsen syndrome; not provided
|FwdALT=C
|FwdREF=G
|GENEINFO=KCNQ1:3784
|GENE_ID=3784
|GENE_NAME=KCNQ1
|REF=G
|RSPOS=2594078
|Reversed=0
|SAO=1
|SSR=0
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD
|VC=SNV
|VP=0x050368000000000002100100
|WGT=0
|dbSNPBuildID=136
|rsid=199472721
}}{{PMID Auto
|PMID=10704188
|Title=Jervell and Lange-Nielsen syndrome: a Norwegian perspective.
}}

{{PMID Auto
|PMID=11530100
|Title=A spectrum of functional effects for disease causing mutations in the Jervell and Lange-Nielsen 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=18752142
|Title=Molecular genetic analysis of long QT syndrome in Norway indicating a high prevalence of heterozygous mutation carriers.
}}