{{Rsnum
|rsid=6873793
|Chromosome=5
|position=3092078
|Orientation=plus
|GMAF=0.494
|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 | 20.4 | 50.4 | 29.2
| HCB | 66.4 | 30.7 | 2.9
| JPT | 68.1 | 30.1 | 1.8
| YRI | 12.9 | 37.4 | 49.7
| ASW | 26.3 | 31.6 | 42.1
| CHB | 66.4 | 30.7 | 2.9
| CHD | 66.1 | 33.9 | 0.0
| GIH | 40.6 | 50.5 | 8.9
| LWK | 5.5 | 38.2 | 56.4
| MEX | 22.4 | 46.6 | 31.0
| MKK | 14.1 | 48.7 | 37.2
| TSI | 14.7 | 48.0 | 37.3
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23166209
  |Trait=QT interval
  |Title=Impact of Ancestry and Common Genetic Variants on QT Interval in African Americans.
  |RiskAllele=C
  |Pval=1E-6
  |OR=1.47
  |ORtxt=[0.88-2.06] unit increase
  |OA=1
}}

{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}