{{Rsnum
|rsid=141813529
|Chromosome=21
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=KCNE1
|position=34449459
|Gene_s=KCNE1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=G
|CHROM=21
|CLNACC=RCV000057842.1
|CLNALLE=1
|CLNDBN=not provided
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=NBK1405:C2676723:612347:768:90647
|CLNHGVS=NC_000021.8:g.35821757A>G
|CLNORIGIN=1
|CLNSIG=1
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=176261.0001
|Disease=not provided
|FwdALT=G
|FwdREF=A
|GENEINFO=KCNE1:3753
|GENE_ID=3753
|GENE_NAME=KCNE1
|REF=A
|RSPOS=35821757
|Reversed=0
|SAO=1
|SSR=0
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD
|VC=SNV
|VP=0x050368000000000002100100
|WGT=0
|dbSNPBuildID=136
|rsid=141813529
}}{{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
}}