{{Rsnum
|rsid=1321311
|Chromosome=6
|position=36655123
|Orientation=minus
|GMAF=0.2475
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 47.3 | 42.9 | 9.8
| HCB | 70.1 | 27.0 | 2.9
| JPT | 71.7 | 27.4 | 0.9
| YRI | 31.3 | 50.3 | 18.4
| ASW | 35.1 | 45.6 | 19.3
| CHB | 70.1 | 27.0 | 2.9
| CHD | 61.5 | 38.5 | 0.0
| GIH | 40.0 | 42.0 | 18.0
| LWK | 24.1 | 52.8 | 23.1
| MEX | 60.3 | 37.9 | 1.7
| MKK | 13.5 | 51.3 | 35.3
| TSI | 64.7 | 28.4 | 6.9
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20062063
|Trait=Electrocardiographic traits
|Title=Several common variants modulate heart rate, PR interval and QRS duration
|RiskAllele=T
|Pval=3E-10
|OR=6.52
|ORtxt=[4.50-8.55] % SD increase
}}

{{PMID Auto
|PMID=22634755
|Title=Common variation near CDKN1A, POLD3 and SHROOM2 influences colorectal cancer risk.
}}

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