{{Rsnum
|rsid=6466479
|Gene=FOXP2
|Chromosome=7
|position=114101050
|Orientation=plus
|GMAF=0.3398
|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 | 0.9 | 18.6 | 80.5
| HCB | 29.9 | 49.6 | 20.4
| JPT | 23.0 | 46.0 | 31.0
| YRI | 38.1 | 47.6 | 14.3
| ASW | 15.8 | 64.9 | 19.3
| CHB | 29.9 | 49.6 | 20.4
| CHD | 25.0 | 61.1 | 13.9
| GIH | 8.9 | 34.7 | 56.4
| LWK | 40.9 | 43.6 | 15.5
| MEX | 1.7 | 24.1 | 74.1
| MKK | 36.5 | 48.7 | 14.7
| TSI | 2.9 | 22.5 | 74.5
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23382691
  |Trait=IgG glycosylation
  |Title=Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.
  |RiskAllele=G
  |Pval=3E-6
  |OR=.22
  |ORtxt=[0.13-0.32] unit decrease
  |OA=1
}}

{{on chip | Affy GenomeWide 6}}