{{Rsnum
|rsid=7006687
|Chromosome=8
|position=18376073
|Orientation=plus
|GMAF=0.4256
|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 | 23.0 | 42.5 | 34.5
| HCB | 16.2 | 55.1 | 28.7
| JPT | 21.2 | 46.9 | 31.9
| YRI | 14.3 | 43.5 | 42.2
| ASW | 15.8 | 47.4 | 36.8
| CHB | 16.2 | 55.1 | 28.7
| CHD | 18.3 | 50.5 | 31.2
| GIH | 27.7 | 51.5 | 20.8
| LWK | 10.2 | 62.0 | 27.8
| MEX | 15.5 | 51.7 | 32.8
| MKK | 21.8 | 54.5 | 23.7
| TSI | 25.5 | 46.1 | 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=T
  |Pval=2E-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}}