{{Rsnum
|rsid=12701937
|Chromosome=7
|position=41782319
|Orientation=plus
|GMAF=0.292
|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 | 29.2 | 53.1 | 17.7
| HCB | 42.6 | 47.1 | 10.3
| JPT | 41.1 | 44.6 | 14.3
| YRI | 99.3 | 0.7 | 0.0
| ASW | 75.4 | 24.6 | 0.0
| CHB | 42.6 | 47.1 | 10.3
| CHD | 49.1 | 39.8 | 11.1
| GIH | 41.6 | 46.5 | 11.9
| LWK | 98.2 | 1.8 | 0.0
| MEX | 50.0 | 41.4 | 8.6
| MKK | 77.6 | 19.9 | 2.6
| TSI | 28.4 | 46.1 | 25.5
| HapMapRevision=28
}}{{PMID Auto
|PMID=23359760
|Title=Single-nucleotide polymorphism associations for colorectal cancer in southern chinese population
|OA=1
}}

{{PMID Auto
|PMID=20610541
|Title=Genome-wide association study for colorectal cancer identifies risk polymorphisms in German familial cases and implicates MAPK signalling pathways in disease susceptibility.
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}