{{Rsnum
|rsid=535586
|Gene=EHMT2
|Chromosome=6
|position=31892560
|Orientation=minus
|GMAF=0.1896
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=EHMT2
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 14.2 | 40.7 | 45.1
| HCB | 2.2 | 38.0 | 59.9
| JPT | 0.0 | 15.9 | 84.1
| YRI | 1.4 | 21.8 | 76.9
| ASW | 1.8 | 21.1 | 77.2
| CHB | 2.2 | 38.0 | 59.9
| CHD | 4.6 | 33.0 | 62.4
| GIH | 3.0 | 33.7 | 63.4
| LWK | 0.9 | 14.5 | 84.5
| MEX | 0.0 | 15.5 | 84.5
| MKK | 3.8 | 30.8 | 65.4
| TSI | 3.9 | 31.4 | 64.7
| HapMapRevision=28
}}{{PMID Auto
|PMID=19843671
|Title=Genetic variants of methyl metabolizing enzymes and epigenetic regulators: associations with promoter CpG island hypermethylation in colorectal cancer
}}

{{PMID Auto
|PMID=19124506
|Title=Common genetic variation in candidate genes and susceptibility to subtypes of breast cancer.
|OA=1
}}

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