{{Rsnum
|rsid=230014
|Chromosome=20
|position=51123323
|Orientation=plus
|GMAF=0.4674
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 25.0 | 48.4 | 26.6
| HCB | 51.1 | 37.8 | 11.1
| JPT | 62.2 | 35.6 | 2.2
| YRI | 1.6 | 14.5 | 83.9
| ASW | 0.0 | 0.0 | 0.0
| CHB | 51.1 | 37.8 | 11.1
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| 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=4E-6
  |OR=NR
  |ORtxt=NR
  }}

{{on chip | HumanOmni1Quad}}