{{Rsnum
|rsid=1321313
|Chromosome=6
|position=36651044
|Orientation=minus
|GMAF=0.1947
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 10.0 | 40.9 | 49.1
| HCB | 3.0 | 27.8 | 69.2
| JPT | 0.9 | 30.9 | 68.2
| YRI | 6.2 | 35.4 | 58.3
| ASW | 7.3 | 30.9 | 61.8
| CHB | 3.0 | 27.8 | 69.2
| CHD | 0.0 | 38.5 | 61.5
| GIH | 17.8 | 42.6 | 39.6
| LWK | 4.6 | 34.3 | 61.1
| MEX | 0.0 | 36.2 | 63.8
| MKK | 11.1 | 43.1 | 45.8
| TSI | 5.0 | 26.7 | 68.3
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23463857
  |Trait=Electrocardiographic conduction measures
  |Title=Genome- and phenome-wide analyses of cardiac conduction identifies markers of arrhythmia risk.
  |RiskAllele=C
  |Pval=5E-25
  |OR=.81
  |ORtxt=[NR] msec decrease
  |OA=1
}}

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