{{Rsnum
|rsid=1612141
|Chromosome=14
|position=41233395
|Orientation=minus
|GMAF=0.2259
|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 | 64.6 | 31.0 | 4.4
| HCB | 66.4 | 29.2 | 4.4
| JPT | 71.7 | 27.4 | 0.9
| YRI | 59.2 | 31.3 | 9.5
| ASW | 66.1 | 28.6 | 5.4
| CHB | 66.4 | 29.2 | 4.4
| CHD | 71.4 | 28.6 | 0.0
| GIH | 83.2 | 15.8 | 1.0
| LWK | 40.9 | 47.3 | 11.8
| MEX | 40.4 | 36.8 | 22.8
| MKK | 41.3 | 46.5 | 12.3
| TSI | 70.7 | 26.3 | 3.0
| 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=5E-6
  |OR=NR
  |ORtxt=NR
  }}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}