{{Rsnum
|rsid=199473457
|Chromosome=11
|position=2572020
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=KCNQ1
|Gene_s=KCNQ1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Orientation=plus
}}{{ClinVar
|ALT=T
|CHROM=11
|CLNACC=RCV000046106.2; RCV000057733.1
|CLNALLE=1
|CLNDBN=KCNQ1-related acquired long QT syndrome; not provided
|CLNDSDB=MedGen
|CLNDSDBID=CN177653
|CLNHGVS=NC_000011.9:g.2593250C>T
|CLNORIGIN=1
|CLNSIG=1
|Disease=KCNQ1-related acquired long QT syndrome; not provided
|FwdALT=T
|FwdREF=C
|GENEINFO=KCNQ1:3784
|GENE_ID=3784
|GENE_NAME=KCNQ1
|REF=C
|RSPOS=2593250
|Reversed=0
|SAO=1
|SSR=0
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD
|VC=SNV
|VP=0x050368000000000002100100
|WGT=0
|dbSNPBuildID=136
|rsid=199473457
}}{{PMID Auto
|PMID=19843
|Title=Eschaemia during arterial reconstructive surgery. Biochemical changes as reflected in popliteal vein samples.
}}

{{PMID Auto
|PMID=12205790
|Title=[Congenital long QT syndrome in newborns].
}}

{{PMID Auto
|PMID=14998624
|Title=Long QT syndrome in neonates: conduction disorders associated with HERG mutations and sinus bradycardia with KCNQ1 mutations.
}}

{{PMID Auto
|PMID=15176425
|Title=Four potassium channel mutations account for 73% of the genetic spectrum underlying long-QT syndrome (LQTS) and provide evidence for a strong founder effect in Finland.
}}

{{PMID Auto
|PMID=16922724
|Title=Spectrum of pathogenic mutations and associated polymorphisms in a cohort of 44 unrelated patients with long QT syndrome.
}}

{{PMID Auto
|PMID=19716085
|Title=Spectrum and prevalence of mutations from the first 2,500 consecutive unrelated patients referred for the FAMILION long QT syndrome genetic test.
|OA=1
}}