{{Rsnum
|rsid=120074185
|Chromosome=11
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=KCNQ1
|position=2776032
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=KCNQ1
}}{{omim
|id=607542
|rsnum=120074185
|variant=0015
}}{{ClinVar
|rsid=120074185
|Reversed=0
|FwdREF=C
|FwdALT=A,T
|REF=C
|ALT=A,T
|RSPOS=2797262
|CHROM=11
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050168000000000002110100
|GENEINFO=KCNQ1:3784
|GENE_NAME=KCNQ1
|GENE_ID=3784
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000011.9:g.2797262C>A; NC_000011.9:g.2797262C>T
|CLNORIGIN=1
|CLNSRCID=
607542.0015
|CLNSIG=5
|CLNCUI=
|CLNACC=
RCV000057612.1; RCV000003274.1; RCV000046011.2; RCV000057613.1
|Tags=PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDBN=not provided; Long QT syndrome 1; Long QT syndrome, LQT1 subtype
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT; MedGen
|CLNDSDBID=NBK1129:NBK1405:C0035828:192500:101016:20852007; CN177655
|CLNSRC=OMIM Allelic Variant
|Disease=not provided; Long QT syndrome 1; Long QT syndrome
}}{{PMID Auto
|PMID=9386136
|Title=KVLQT1 C-terminal missense mutation causes a forme fruste long-QT syndrome.
}}

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

{{PMID Auto
|PMID=14760488
|Title=Genetic variations of KCNQ1, KCNH2, SCN5A, KCNE1, and KCNE2 in drug-induced long QT syndrome patients.
}}

{{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=18174212
|Title=Kv7.1 (KCNQ1) properties and channelopathies.
|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
}}