{{Rsnum
|rsid=17137124
|Gene=FOXP2
|Chromosome=7
|position=114570759
|Orientation=plus
|GMAF=0.4692
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=FOXP2
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 37.2 | 42.5 | 20.4
| HCB | 56.9 | 32.8 | 10.2
| JPT | 54.9 | 39.8 | 5.3
| YRI | 4.8 | 30.6 | 64.6
| ASW | 8.9 | 28.6 | 62.5
| CHB | 56.9 | 32.8 | 10.2
| CHD | 55.0 | 36.7 | 8.3
| GIH | 42.0 | 45.0 | 13.0
| LWK | 9.1 | 43.6 | 47.3
| MEX | 32.8 | 55.2 | 12.1
| MKK | 8.3 | 44.2 | 47.4
| TSI | 19.6 | 52.0 | 28.4
| HapMapRevision=28
}}{{PMID|15877281|OA=1
}} variations in [[rs17137124]] and [[rs10227893]] may impair speech

{{PMID Auto
|PMID=22129783
|Title=FOXP2, APOE, and PRNP: New Modulators in Primary Progressive Aphasia
}}

{{PMID Auto
|PMID=19997522
|Title=Convergent genetic linkage and associations to language, speech and reading measures in families of probands with Specific Language Impairment.
|OA=1
}}

{{PMID Auto
|PMID=20649982
|Title=FOXP2 gene and language impairment in schizophrenia: association and epigenetic studies.
|OA=1
}}

{{PMID Auto
|PMID=20858950
|Title=The speech and language FOXP2 gene modulates the phenotype of frontotemporal lobar degeneration.
}}

{{PMID Auto
|PMID=20923434
|Title=Association between FOXP2 gene and speech sound disorder in Chinese population.
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}