{{Rsnum
|rsid = 17221854
|Status = Deleted
|Orientation=plus
|ReferenceAllele=C
|MissenseAllele=T
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Chromosome=11
|position=2777990
|Gene=KCNQ1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=KCNQ1
}}{{omim
|desc=LONG QT SYNDROME 1
|id=607542
|rsnum=17221854
|variant=0031
}}

{{ClinVar
|rsid=17221854
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=2799220
|CHROM=11
|dbSNPBuildID=127
|SSR=0
|SAO=1
|VP=0x050178000000000002110100
|GENEINFO=KCNQ1:3784
|GENE_NAME=KCNQ1
|GENE_ID=3784
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.2799220C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=607542.0031
|CLNSIG=255
|CLNCUI=C0035828
|CLNDBN=Long QT syndrome 1; Acquired susceptibility to long QT syndrome 1; KCNQ1-related acquired long QT syndrome; Long QT syndrome, LQT1 subtype; not provided
|Disease=Long QT syndrome 1; Acquired susceptibility to long QT syndrome 1; KCNQ1-related acquired long QT syndrome; Long QT syndrome; not provided
|CLNACC=RCV000003291.1; RCV000003292.1; RCV000046023.2; RCV000046024.2; RCV000057628.1
|Tags=PM;TPA;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT; MedGen
|CLNDSDBID=NBK1129:NBK1405:C0035828:192500:101016:20852007; C1843738; CN177653; CN177655
}}

{{PMID Auto
|PMID=19214780
|Title=In silico investigations on functional and haplotype tag SNPs associated with congenital long QT syndromes (LQTSs).
|OA=1
}}

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

{{PMID Auto
|PMID=11997281
|Title=Allelic variants in long-QT disease genes in patients with drug-associated torsades de pointes.
}}

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

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}