{{Rsnum
|rsid=1805127
|Gene=KCNE1
|Chromosome=21
|position=34449523
|Orientation=minus
|GMAF=0.3315
|Gene_s=KCNE1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 10.7 | 49.1 | 40.2
| HCB | 9.6 | 46.3 | 44.1
| JPT | 8.0 | 41.1 | 50.9
| YRI | 4.8 | 43.5 | 51.7
| ASW | 8.8 | 35.1 | 56.1
| CHB | 9.6 | 46.3 | 44.1
| CHD | 3.7 | 46.3 | 50.0
| GIH | 9.0 | 46.0 | 45.0
| LWK | 7.3 | 37.3 | 55.5
| MEX | 13.8 | 43.1 | 43.1
| MKK | 3.2 | 33.3 | 63.5
| TSI | 14.7 | 53.9 | 31.4
| HapMapRevision=28
}}{{ClinVar
|rsid=1805127
|Reversed=1
|FwdREF=A
|FwdALT=G
|REF=T
|ALT=C
|RSPOS=35821821
|CHROM=21
|dbSNPBuildID=89
|SSR=0
|SAO=1
|VP=0x05037800000015051f100100
|GENEINFO=KCNE1:3753
|GENE_NAME=KCNE1
|GENE_ID=3753
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000021.8:g.35821821T>C
|CLNORIGIN=1
|CLNSIG=2
|Tags=RV;PM;TPA;PMC;S3D;SLO;VLD;G5;HD;GNO;KGPhase1;KGPilot123;KGPROD;OTHERKG;PH3;LSD
|CAF=0.3315; 0.6685
|CLNACC=RCV000035351.1; RCV000057834.1
|CLNDBN=AllHighlyPenetrant; not provided
|CLNDSDB=MedGen
|CLNDSDBID=CN169374
|COMMON=1
|Disease=AllHighlyPenetrant; not provided
}}

{{PMID Auto
|PMID=17227789
|Title=The common non-synonymous variant G38S of the KCNE1-(minK)-gene is not associated to QT interval in Central European Caucasians: results from the KORA study.
}}

{{PMID Auto
|PMID=17534376
|Title=Confirmation of associations between ion channel gene SNPs and QTc interval duration in healthy subjects.
|OA=1
}}

{{PMID Auto
|PMID=18520591
|Title=Sequence variants in host cell factor C1 are associated with Meniere's disease.
|OA=1
}}

{{PMID Auto
|PMID=18674739
|Title=Effect of common KCNE1 and SCN5A ion channel gene variants on T-wave alternans, a marker of cardiac repolarization, during clinical exercise stress test: the Finnish Cardiovascular Study.
}}

{{PMID Auto
|PMID=19019189
|Title=Common candidate gene variants are associated with QT interval duration in the general population.
|OA=1
}}

{{PMID Auto
|PMID=19660109
|Title=Positive selection at codon 38 of the human KCNE1 (= minK) gene and sporadic absence of 38Ser-coding mRNAs in Gly38Ser heterozygotes.
|OA=1
}}

{{PMID Auto
|PMID=21811988
|Title=[Association of rs1805127 polymorphism of KCNE1 gene with atrial fibrillation in Uigur population of Xinjiang].
}}

{{PMID Auto
|PMID=17210
|Title=[Carbogen therapy of acute cochlear disorders].
}}

{{PMID Auto
|PMID=12402336
|Title=DHPLC analysis of potassium ion channel genes in congenital long QT syndrome.
}}

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

{{PMID Auto
|PMID=16487223
|Title=Genetic polymorphisms in KCNQ1, HERG, KCNE1 and KCNE2 genes in the Chinese, Malay and Indian populations of Singapore.
|OA=1
}}

{{PMID Auto
|PMID=17597962
|Title=Mutation screening in KCNQ1, HERG, KCNE1, KCNE2 and SCN5A genes in a long QT syndrome family.
}}

{{PMID Auto
|PMID=18426444
|Title=Single nucleotide polymorphisms and haplotype of four genes encoding cardiac ion channels in Chinese and their association with arrhythmia.
}}

{{PMID Auto
|PMID=23874724
|Title=KCNE1 rs1805127 Polymorphism Increases the Risk of Atrial Fibrillation: A Meta-Analysis of 10 Studies
|OA=1
}}

{{PMID Auto
|PMID=22934933
|Title=A replication study on proposed candidate genes in Meniere's disease, and a review of the current status of genetic studies.
}}

{{PMID Auto
|PMID=23020083
|Title=Association of KCNE1 genetic polymorphisms with atrial fibrillation in a Chinese Han population.
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}