{{Rsnum
|rsid=6691170
|Chromosome=1
|position=221872104
|Orientation=plus
|GMAF=0.2608
|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 | 42.5 | 37.2 | 20.4
| HCB | 96.2 | 3.8 | 0.0
| JPT | 96.3 | 3.7 | 0.0
| YRI | 41.0 | 50.7 | 8.3
| ASW | 53.6 | 32.1 | 14.3
| CHB | 96.2 | 3.8 | 0.0
| CHD | 99.0 | 1.0 | 0.0
| GIH | 51.0 | 43.0 | 6.0
| LWK | 41.7 | 52.8 | 5.6
| MEX | 55.4 | 35.7 | 8.9
| MKK | 49.7 | 43.2 | 7.1
| TSI | 29.7 | 53.5 | 16.8
| 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=T
|Pval=1E-9
|OR=1.0600
|ORtxt=[1.03-1.09]
}}

{{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=22629442
|Title=Evaluation of Allele-Specific Somatic Changes of Genome-Wide Association Study Susceptibility Alleles in Human Colorectal Cancers
|OA=1
}}

{{PMID Auto
|PMID=22675446
|Title=Colorectal Cancer Linkage on Chromosomes 4q21, 8q13, 12q24, and 15q22
|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 | Illumina Human 1M}}