{{Rsnum
|rsid=10890920
|Chromosome=11
|position=109002392
|Orientation=plus
|GMAF=0.4972
|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 | 34.5 | 45.1 | 20.4
| HCB | 44.9 | 41.9 | 13.2
| JPT | 36.3 | 52.2 | 11.5
| YRI | 6.8 | 27.2 | 66.0
| ASW | 12.3 | 50.9 | 36.8
| CHB | 44.9 | 41.9 | 13.2
| CHD | 37.6 | 39.4 | 22.9
| GIH | 33.7 | 35.6 | 30.7
| LWK | 0.9 | 24.5 | 74.5
| MEX | 31.0 | 43.1 | 25.9
| MKK | 5.8 | 39.1 | 55.1
| TSI | 26.5 | 45.1 | 28.4
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23459443
  |Trait=QT interval (interaction)
  |Title=Drug-gene interactions and the search for missing heritability: a cross-sectional pharmacogenomics study of the QT interval.
  |RiskAllele=A
  |Pval=3E-6
  |OR=NR
  |ORtxt=NR
  }}

{{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}}