{{Rsnum
|rsid=1229761
|Gene=FOXP2
|Chromosome=7
|position=114583668
|Orientation=minus
|GMAF=0.2043
|Gene_s=FOXP2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 15.0 | 38.9 | 46.0
| HCB | 0.0 | 5.1 | 94.9
| JPT | 0.0 | 1.8 | 98.2
| YRI | 0.0 | 19.7 | 80.3
| ASW | 7.0 | 35.1 | 57.9
| CHB | 0.0 | 5.1 | 94.9
| CHD | 0.0 | 2.8 | 97.2
| GIH | 5.0 | 25.7 | 69.3
| LWK | 0.0 | 21.8 | 78.2
| MEX | 0.0 | 37.9 | 62.1
| MKK | 1.9 | 28.8 | 69.2
| TSI | 20.6 | 49.0 | 30.4
| HapMapRevision=28
}}{{PMID Auto
|PMID=22504457
|Title=An association study of sequence variants in the forkhead box P2 (FOXP2) gene and adulthood attention-deficit/hyperactivity disorder in two European samples
}}

{{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}}