{{Rsnum
|rsid=387906290
|Chromosome=11
|position=2583434
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=KCNQ1
|Gene_s=KCNQ1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=C
|CHROM=11
|CLNACC=RCV000003282.1; RCV000046158.2
|CLNALLE=1
|CLNDBN=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
|CLNHGVS=NC_000011.9:g.2604664G>C
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=607542.0023
|Disease=Long QT syndrome 1; Long QT syndrome
|FwdALT=C
|FwdREF=G
|REF=G
|RSPOS=2604664
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=387906290
|GENEINFO=KCNQ1:3784
|GENE_ID=3784
|GENE_NAME=KCNQ1
}}