{{Rsnum
|rsid=120074189
|Chromosome=11
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=KCNQ1
|position=2778003
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=KCNQ1
}}{{omim
|id=607542
|rsnum=120074189
|variant=0027
}}{{ClinVar
|rsid=120074189
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=2799233
|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
|CLNHGVS=NC_000011.9:g.2799233C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=607542.0027
|CLNSIG=5
|CLNCUI=C0022387
|CLNDBN=Jervell and Lange-Nielsen syndrome; Long QT syndrome, LQT1 subtype; not provided
|Disease=Jervell and Lange-Nielsen syndrome; Long QT syndrome; not provided
|CLNACC=RCV000003286.1; RCV000046026.2; RCV000057632.1
|Tags=PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet:SNOMED_CT; MedGen
|CLNDSDBID=NBK1405:C0022387:220400:768:90647:373905003; CN177655
}}{{PMID Auto
|PMID=173292
|Title=Oxidase-peroxidase enzymes of Datura innoxia. Oxidation of reduced nicotinamide-adenine dinucleotide in the presence of formylphenylacetic acid ethyl ester.
|OA=1
}}

{{PMID Auto
|PMID=9799083
|Title=Genomic organization and mutational analysis of KVLQT1, a gene responsible for familial long QT syndrome.
}}

{{PMID Auto
|PMID=10024302
|Title=Genomic organization of the KCNQ1 K+ channel gene and identification of C-terminal mutations in the long-QT syndrome.
}}

{{PMID Auto
|PMID=11162126
|Title=Characterization and subcellular localization of KCNQ1 with a heterozygous mutation in the C terminus.
}}

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

{{PMID Auto
|PMID=15840476
|Title=Compendium of cardiac channel mutations in 541 consecutive unrelated patients referred for long QT syndrome genetic testing.
}}