{{Rsnum
|rsid=199472713
|Chromosome=11
|position=2572056
|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=A,T
|CHROM=11
|CLNACC=RCV000057740.1; RCV000046111.2; RCV000057741.1
|CLNALLE=1; 2
|CLNDBN=not provided; Long QT syndrome, LQT1 subtype
|CLNDSDB=MedGen
|CLNDSDBID=CN177655
|CLNHGVS=NC_000011.9:g.2593286C>A; NC_000011.9:g.2593286C>T
|CLNORIGIN=1
|CLNSIG=1
|Disease=not provided; Long QT syndrome
|FwdALT=A,T
|FwdREF=C
|GENEINFO=KCNQ1:3784
|GENE_ID=3784
|GENE_NAME=KCNQ1
|REF=C
|RSPOS=2593286
|Reversed=0
|SAO=1
|SSR=0
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD
|VC=SNV
|VP=0x050368000000000002100100
|WGT=0
|dbSNPBuildID=136
|rsid=199472713
}}{{PMID Auto
|PMID=15466
|Title=Analysis of employment turnover and job satisfaction of physician's assistants graduated from the Physician's Assistant Program of the University of Alabama in Birmingham, 1972-1975.
}}

{{PMID Auto
|PMID=10409658
|Title=Long QT syndrome-associated mutations in the S4-S5 linker of KvLQT1 potassium channels modify gating and interaction with minK subunits.
}}

{{PMID Auto
|PMID=10973849
|Title=Spectrum of mutations in long-QT syndrome genes. KVLQT1, HERG, SCN5A, KCNE1, and KCNE2.
}}

{{PMID Auto
|PMID=12877697
|Title=Catecholamine-provoked microvoltage T wave alternans in genotyped long QT syndrome.
}}

{{PMID Auto
|PMID=14678125
|Title=Location of mutation in the KCNQ1 and phenotypic presentation of long QT syndrome.
}}

{{PMID Auto
|PMID=15028050
|Title=Additional gene variants reduce effectiveness of beta-blockers in the LQT1 form of long QT syndrome.
}}

{{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.
}}