{{Rsnum
|rsid=10916248
|Chromosome=1
|position=224068646
|Orientation=plus
|GMAF=0.2305
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;T)
| geno3=(T;T)
| CEU | 57.1 | 39.3 | 3.6
| HCB | 35.0 | 46.7 | 18.2
| JPT | 42.5 | 48.7 | 8.8
| YRI | 82.3 | 16.3 | 1.4
| ASW | 77.2 | 21.1 | 1.8
| CHB | 35.0 | 46.7 | 18.2
| CHD | 31.2 | 49.5 | 19.3
| GIH | 79.2 | 15.8 | 5.0
| LWK | 76.4 | 22.7 | 0.9
| MEX | 44.8 | 46.6 | 8.6
| MKK | 71.8 | 27.6 | 0.6
| TSI | 60.8 | 32.4 | 6.9
| 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 | Affy GenomeWide 6}}