{{Rsnum
|rsid=6687758
|Chromosome=1
|position=221991606
|Orientation=plus
|GMAF=0.2153
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 61.9 | 34.5 | 3.5
| HCB | 61.3 | 35.0 | 3.6
| JPT | 46.4 | 42.9 | 10.7
| YRI | 70.7 | 27.2 | 2.0
| ASW | 63.2 | 33.3 | 3.5
| CHB | 61.3 | 35.0 | 3.6
| CHD | 71.6 | 27.5 | 0.9
| GIH | 78.2 | 20.8 | 1.0
| LWK | 67.3 | 28.2 | 4.5
| MEX | 51.7 | 46.6 | 1.7
| MKK | 73.1 | 23.7 | 3.2
| TSI | 55.9 | 40.2 | 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=G
|Pval=2E-9
|OR=1.0900
|ORtxt=[1.06-1.12]
}}

{{PMID Auto GWAS
|PMID=21685912
|Trait=None
|Title=Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy.
|RiskAllele=
|Pval=6E-8
|OR=1.2700
|ORtxt=[1.16-1.39]
|OA=1
}}

{{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=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 | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}