{{Rsnum
|rsid=120074183
|Chromosome=11
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=KCNQ1
|position=2585213
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=KCNQ1
}}{{omim
|id=607542
|rsnum=120074183
|variant=0011
}}{{ClinVar
|rsid=120074183
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=2606443
|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.2606443G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=607542.0011
|CLNSIG=5
|CLNCUI=C0035828
|CLNDBN=Long QT syndrome 1; Long QT syndrome, LQT1 subtype; not provided
|Disease=Long QT syndrome 1; Long QT syndrome; not provided
|CLNACC=RCV000003270.1; RCV000045944.2; RCV000057536.1
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT; MedGen
|CLNDSDBID=NBK1129:NBK1405:C0035828:192500:101016:20852007; CN177655
}}{{PMID Auto
|PMID=8528244
|Title=Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias.
}}

{{PMID Auto
|PMID=10376919
|Title=Functional effects of mutations in KvLQT1 that cause long QT syndrome.
}}

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