{{Rsnum
|rsid=2663905
|Chromosome=15
|position=81066796
|Orientation=plus
|GMAF=0.3095
|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 | 62.7 | 25.4 | 11.9
| HCB | 19.5 | 43.9 | 36.6
| JPT | 23.3 | 44.2 | 32.6
| YRI | 89.5 | 10.5 | 0.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 19.5 | 43.9 | 36.6
| 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=5E-6
  |OR=NR
  |ORtxt=NR
  }}