{{Rsnum
|rsid=2896218
|Gene=WNT2
|Chromosome=7
|position=117279924
|Orientation=plus
|GMAF=0.3806
|Gene_s=WNT2
|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 | 27.4 | 52.2 | 20.4
| HCB | 44.0 | 47.8 | 8.2
| JPT | 48.2 | 42.9 | 8.9
| YRI | 44.9 | 42.2 | 12.9
| ASW | 37.5 | 53.6 | 8.9
| CHB | 44.0 | 47.8 | 8.2
| CHD | 0.0 | 0.0 | 0.0
| GIH | 38.0 | 41.0 | 21.0
| LWK | 38.0 | 39.8 | 22.2
| MEX | 48.3 | 44.8 | 6.9
| MKK | 20.3 | 50.3 | 29.4
| TSI | 30.7 | 53.5 | 15.8
| HapMapRevision=28
}}{{PMID Auto
|PMID=22522212
|Title=The WNT2 gene polymorphism associated with speech delay inherent to autism
}}

{{PMID Auto
|PMID=21575668
|Title=Association study of the CNS patterning genes and autism in Han Chinese in Taiwan.
}}

{{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}}