{{Rsnum
|rsid=5934683
|Chromosome=X
|position=9783434
|Orientation=plus
|GMAF=0.3736
|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 | 50.4 | 27.4 | 22.1
| HCB | 10.2 | 10.9 | 78.8
| JPT | 6.3 | 12.6 | 81.1
| YRI | 11.6 | 17.0 | 71.4
| ASW | 17.5 | 28.1 | 54.4
| CHB | 10.2 | 10.9 | 78.8
| CHD | 9.2 | 18.3 | 72.5
| GIH | 32.7 | 19.8 | 47.5
| LWK | 9.1 | 22.7 | 68.2
| MEX | 39.7 | 22.4 | 37.9
| MKK | 18.1 | 21.3 | 60.6
| TSI | 50.0 | 15.7 | 34.3
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=22634755
|Trait=None
|Title=Common variation near CDKN1A, POLD3 and SHROOM2 influences colorectal cancer risk.
|RiskAllele=
|Pval=7E-10
|OR=1.0700
|ORtxt=None
}}

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