{{Rsnum
|rsid=6755560
|Chromosome=2
|position=206853059
|Orientation=plus
|GMAF=0.2052
|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 | 9.7 | 39.8 | 50.4
| HCB | 0.0 | 4.4 | 95.6
| JPT | 0.0 | 5.3 | 94.7
| YRI | 4.1 | 23.1 | 72.8
| ASW | 3.5 | 35.1 | 61.4
| CHB | 0.0 | 4.4 | 95.6
| CHD | 0.0 | 8.3 | 91.7
| GIH | 1.0 | 36.6 | 62.4
| LWK | 0.0 | 30.9 | 69.1
| MEX | 17.2 | 34.5 | 48.3
| MKK | 3.2 | 35.3 | 61.5
| TSI | 18.6 | 40.2 | 41.2
| 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 | Affy GenomeWide 6}}
{{on chip | FTDNA}}