{{Rsnum
|rsid=10227893
|Gene=FOXP2
|Chromosome=7
|position=114630022
|Orientation=plus
|GMAF=0.118
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene_s=FOXP2
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 0.0 | 11.5 | 88.5
| HCB | 0.0 | 0.0 | 100.0
| JPT | 0.0 | 0.0 | 100.0
| YRI | 8.2 | 40.1 | 51.7
| ASW | 12.5 | 46.4 | 41.1
| CHB | 0.0 | 0.0 | 100.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 1.0 | 13.9 | 85.1
| LWK | 9.3 | 44.4 | 46.3
| MEX | 3.5 | 12.3 | 84.2
| MKK | 12.8 | 51.3 | 35.9
| TSI | 0.0 | 12.9 | 87.1
| HapMapRevision=28
}}{{PMID|15877281|OA=1
}} variations in [[rs17137124]] and [[rs10227893]] may impair speech

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