{{Rsnum
|rsid=193922365
|Chromosome=11
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=KCNQ1
|position=2572970
|Gene_s=KCNQ1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=193922365
|Reversed=0
|FwdREF=C
|FwdALT=A,T
|REF=C
|ALT=A,T
|RSPOS=2594200
|CHROM=11
|dbSNPBuildID=136
|SSR=0
|SAO=1
|VP=0x050368000000000002100100
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000011.9:g.2594200C>A; NC_000011.9:g.2594200C>T
|CLNSRC=Correlagen
|CLNORIGIN=1
|CLNSIG=4
|CLNCUI=
|CLNDBN=not provided; Long QT syndrome
|Disease=not provided; Long QT syndrome
|CLNACC=
RCV000057791.1; RCV000030111.1; RCV000057792.1
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD
|CLNDSDB=MedGen:SNOMED_CT
|CLNDSDBID=C0023976:9651007
|GENEINFO=KCNQ1:3784
|GENE_ID=3784
|GENE_NAME=KCNQ1
}}{{PMID Auto
|PMID=20486
|Title=Early effects of hypervitaminosis A on gluconeogenic activity and amino acid metabolizing enzymes of rat liver.
}}

{{PMID Auto
|PMID=15466642
|Title=Spectrum and frequency of cardiac channel defects in swimming-triggered arrhythmia syndromes.
}}

{{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=17905336
|Title=Long QT and Brugada syndrome gene mutations in New Zealand.
}}

{{PMID Auto
|PMID=19490272
|Title=Mutations in conserved amino acids in the KCNQ1 channel and risk of cardiac events in type-1 long-QT syndrome.
}}

{{PMID Auto
|PMID=19808498
|Title=Biophysical properties of 9 KCNQ1 mutations associated with long-QT syndrome.
|OA=1
}}

{{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
}}