{{Rsnum
|rsid=10784762
|Chromosome=12
|position=69130143
|Orientation=plus
|GMAF=0.3953
|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 | 14.3 | 47.3 | 38.4
| HCB | 5.1 | 39.7 | 55.1
| JPT | 5.3 | 35.4 | 59.3
| YRI | 24.5 | 48.3 | 27.2
| ASW | 28.1 | 50.9 | 21.1
| CHB | 5.1 | 39.7 | 55.1
| CHD | 7.3 | 39.4 | 53.2
| GIH | 10.0 | 45.0 | 45.0
| LWK | 24.8 | 46.8 | 28.4
| MEX | 28.1 | 42.1 | 29.8
| MKK | 21.9 | 51.0 | 27.1
| TSI | 18.6 | 52.0 | 29.4
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23534349
  |Trait=QRS duration
  |Title=Generalization of Variants Identified by Genome-Wide Association Studies for Electrocardiographic Traits in African Americans.
  |RiskAllele=T
  |Pval=6E-6
  |OR=2.38
  |ORtxt=[NR] ms decrease
  }}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}