{{Rsnum
|rsid=760419
|Gene=KCNQ1
|Chromosome=11
|position=2662127
|Orientation=plus
|GMAF=0.4959
|Gene_s=KCNQ1,KCNQ1OT1
|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 | 33.0 | 47.3 | 19.6
| HCB | 42.6 | 47.8 | 9.6
| JPT | 34.8 | 43.8 | 21.4
| YRI | 2.1 | 15.2 | 82.8
| ASW | 7.0 | 47.4 | 45.6
| CHB | 42.6 | 47.8 | 9.6
| CHD | 45.9 | 42.2 | 11.9
| GIH | 35.6 | 48.5 | 15.8
| LWK | 1.8 | 34.9 | 63.3
| MEX | 41.4 | 53.4 | 5.2
| MKK | 10.3 | 44.9 | 44.9
| TSI | 37.3 | 39.2 | 23.5
| HapMapRevision=28
}}{{PMID Auto
|PMID=23651960
|Title=[KCNQ1 mutation in patients with lone atrial fibrillation]
}}

{{PMID Auto
|PMID=16839189
|Title=Human imprinted chromosomal regions are historical hot-spots of recombination.
|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}}