{{Rsnum
|rsid=120074193
|Chromosome=11
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=KCNQ1
|position=2572870
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=KCNQ1
}}{{omim
|id=607542
|rsnum=120074193
|variant=0033
}}{{ClinVar
|rsid=120074193
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=2594100
|CHROM=11
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050368000000000002110100
|GENEINFO=KCNQ1:3784
|GENE_NAME=KCNQ1
|GENE_ID=3784
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.2594100G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=607542.0033
|CLNSIG=5
|CLNCUI=C0035828
|CLNDBN=Long QT syndrome 1; not provided
|Disease=Long QT syndrome 1; not provided
|CLNACC=RCV000003294.1; RCV000057765.1
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1129:NBK1405:C0035828:192500:101016:20852007
}}{{PMID|15466}} 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|10560595}} Swimming, a gene-specific arrhythmogenic trigger for inherited long QT syndrome.

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

{{PMID|12205113|OA=1
}} Mutation in KCNQ1 that has both recessive and dominant characteristics.

{{PMID|12702160|OA=1
}} KCNQ1 mutations in patients with a family history of lethal cardiac arrhythmias and sudden death.

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