{{Rsnum
|rsid=12296050
|Gene=KCNQ1
|Chromosome=11
|position=2468112
|Orientation=plus
|GMAF=0.371
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=KCNQ1
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 63.7 | 35.4 | 0.9
| HCB | 40.1 | 43.1 | 16.8
| JPT | 39.8 | 46.0 | 14.2
| YRI | 17.7 | 49.0 | 33.3
| ASW | 22.8 | 47.4 | 29.8
| CHB | 40.1 | 43.1 | 16.8
| CHD | 39.4 | 42.2 | 18.3
| GIH | 35.6 | 45.5 | 18.8
| LWK | 6.4 | 53.6 | 40.0
| MEX | 51.7 | 37.9 | 10.3
| MKK | 9.0 | 39.1 | 51.9
| TSI | 62.7 | 29.4 | 7.8
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=19305409
|Trait=QT interval
|Title=Common variants at ten loci modulate the QT interval duration in the QTSCD Study
|RiskAllele=T
|Pval=3E-17
|OR=1.44
|ORtxt=[0.95-1.93] ms increase
|OA=1
}}

{{PharmGKB
|RSID=rs12296050
|Name_s=
|Gene_s=KCNQ1
|Feature=
|Evidence=PubMed ID:19305409; Web Resource:http://www.genome.gov/gwastudies/
|Annotation=GWAS results: Common variants at ten loci modulate the QT interval duration in the QTSCD Study. (Initial Sample Size: 15,842 individuals; Replication Sample Size: up to 13,602 individuals); (Region: 11p15.5; Reported Gene(s): KCNQ1; Risk Allele: rs12296050-T); (p-value= 0.00000000000000003).This variant is associated with QT interval.
|Drugs=
|Drug Classes=
|Diseases=
|Curation Level=Non-Curated
|PharmGKB Accession ID=PA164739900
}}

{{PMID Auto GWAS
|PMID=20062063
|Trait=Electrocardiographic traits
|Title=Several common variants modulate heart rate, PR interval and QRS duration
|RiskAllele=T
|Pval=8E-11
|OR=13.16
|ORtxt=[9.19-17.12] % SD increase
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs12296050
|overall_frequency_n=52
|overall_frequency_d=128
|overall_frequency=0.40625
|n_genomes=38
|n_genomes_annotated=0
|n_haplomes=46
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|in_pharmgkb=Y
|autoscore=2
|webscore=N
}}

{{PMID Auto
|PMID=23692438
|Title=Association between KCNQ1 genetic variants and QT interval in a Chinese population.
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Illumina Human 1M}}