{{Rsnum
|rsid=9375225
|Chromosome=6
|position=98140878
|Orientation=plus
|GMAF=0.4045
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 24.6 | 49.2 | 26.2
| HCB | 26.8 | 65.9 | 7.3
| JPT | 48.8 | 41.9 | 9.3
| YRI | 60.4 | 35.8 | 3.8
| ASW | 0.0 | 0.0 | 0.0
| CHB | 26.8 | 65.9 | 7.3
| 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=T
  |Pval=6E-6
  |OR=NR
  |ORtxt=NR
  }}