{{Rsnum
|rsid=2228946
|Gene=WNT2
|Chromosome=7
|position=117278031
|Orientation=minus
|GMAF=0.1919
|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 | 6.2 | 35.7 | 58.0
| HCB | 0.0 | 3.6 | 96.4
| JPT | 0.0 | 1.8 | 98.2
| YRI | 12.9 | 46.9 | 40.1
| ASW | 10.5 | 31.6 | 57.9
| CHB | 0.0 | 3.6 | 96.4
| CHD | 0.0 | 3.7 | 96.3
| GIH | 2.0 | 21.8 | 76.2
| LWK | 12.7 | 50.9 | 36.4
| MEX | 5.2 | 19.0 | 75.9
| MKK | 13.5 | 50.3 | 36.1
| TSI | 3.9 | 30.4 | 65.7
| HapMapRevision=28
}}{{PMID Auto
|PMID=22522212
|Title=The WNT2 gene polymorphism associated with speech delay inherent to autism
}}

{{PMID Auto
|PMID=19838307
|Title=Human placental-specific epipolymorphism and its association with adverse pregnancy outcomes.
|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 | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}