{{Rsnum
|rsid=12548021
|Chromosome=8
|position=29486945
|Orientation=plus
|GMAF=0.3058
|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 | 41.6 | 46.9 | 11.5
| HCB | 62.0 | 29.9 | 8.0
| JPT | 55.8 | 35.4 | 8.8
| YRI | 74.8 | 23.1 | 2.0
| ASW | 68.4 | 29.8 | 1.8
| CHB | 62.0 | 29.9 | 8.0
| CHD | 57.4 | 38.0 | 4.6
| GIH | 47.5 | 46.5 | 5.9
| LWK | 55.0 | 34.9 | 10.1
| MEX | 29.3 | 46.6 | 24.1
| MKK | 66.7 | 31.4 | 1.9
| TSI | 48.0 | 38.2 | 13.7
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23350875
  |Trait=Colorectal cancer
  |Title=A colorectal cancer genome-wide association study in a Spanish cohort identifies two variants associated with colorectal cancer risk at 1p33 and 8p12.
  |RiskAllele=
  |Pval=3E-6
  |OR=1.28
  |ORtxt=[1.155-1.418]
  |OA=1
}}

{{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}}