{{Rsnum
|rsid=6460013
|Gene=EN2
|Chromosome=7
|position=155459499
|Orientation=plus
|GMAF=0.101
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene_s=EN2
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 90.8 | 9.2 | 0.0
| HCB | 91.1 | 8.9 | 0.0
| JPT | 86.4 | 13.6 | 0.0
| YRI | 57.1 | 34.9 | 7.9
| ASW | 0.0 | 0.0 | 0.0
| CHB | 91.1 | 8.9 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| 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=19270442
|Title=Haplotype analysis of the engrailed-2 gene in young-onset Parkinson's disease
}}

{{PMID Auto
|PMID=22522212
|Title=The WNT2 gene polymorphism associated with speech delay inherent to autism
}}

{{PMID|16252243|OA=1
}} Support for the homeobox transcription factor gene ENGRAILED 2 as an autism spectrum disorder susceptibility locus.

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}