{{Rsnum
|rsid=2235356
|Gene=MAPK11
|Chromosome=22
|position=50271920
|Orientation=plus
|GMAF=0.4151
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=MAPK11
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 27.7 | 46.2 | 26.2
| HCB | 39.4 | 46.2 | 14.4
| JPT | 31.2 | 53.2 | 15.6
| YRI | 11.1 | 42.9 | 46.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 39.4 | 46.2 | 14.4
| CHD | 38.7 | 50.9 | 10.4
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{PMID Auto
|PMID=23946768
|Title=A genetic variation of the p38β promoter region is correlated with an increased risk of sporadic colorectal cancer
|OA=1
}}

{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}