{{Rsnum
|rsid=11169552
|Chromosome=12
|position=50761880
|Orientation=plus
|GMAF=0.2369
|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 | 65.5 | 31.0 | 3.5
| HCB | 45.3 | 43.8 | 10.9
| JPT | 54.0 | 37.2 | 8.8
| YRI | 92.5 | 7.5 | 0.0
| ASW | 87.7 | 12.3 | 0.0
| CHB | 45.3 | 43.8 | 10.9
| CHD | 33.3 | 50.0 | 16.7
| GIH | 39.6 | 47.5 | 12.9
| LWK | 71.6 | 26.6 | 1.8
| MEX | 51.7 | 43.1 | 5.2
| MKK | 62.2 | 32.7 | 5.1
| TSI | 74.5 | 21.6 | 3.9
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20972440
|Trait=None
|Title=Meta-analysis of three genome-wide association studies identifies susceptibility loci for colorectal cancer at 1q41, 3q26.2, 12q13.13 and 20q13.33
|RiskAllele=C
|Pval=2E-10
|OR=1.0900
|ORtxt=[1.05-1.11]
}}

{{PMID Auto
|PMID=22076443
|Title=Refinement of the associations between risk of colorectal cancer and polymorphisms on chromosomes 1q41 and 12q13.13
|OA=1
}}

{{PMID Auto
|PMID=22045029
|Title=Relationship between 16 susceptibility loci and colorectal cancer phenotype in 3146 patients.
}}

{{PMID Auto
|PMID=22999960
|Title=Much of the genetic risk of colorectal cancer is likely to be mediated through susceptibility to adenomas.
|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}}