{{Rsnum
|rsid=13072512
|Gene=FOXP1
|Chromosome=3
|position=71364894
|Orientation=plus
|GMAF=0.4986
|Gene_s=FOXP1
|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 | 25.7 | 51.3 | 23.0
| HCB | 9.3 | 34.9 | 55.8
| JPT | 0.0 | 21.6 | 78.4
| YRI | 87.0 | 12.3 | 0.7
| ASW | 68.4 | 29.8 | 1.8
| CHB | 9.3 | 34.9 | 55.8
| CHD | 7.5 | 43.0 | 49.5
| GIH | 13.0 | 52.0 | 35.0
| LWK | 89.0 | 9.2 | 1.8
| MEX | 21.1 | 50.9 | 28.1
| MKK | 64.3 | 29.9 | 5.8
| TSI | 22.8 | 49.5 | 27.7
| 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=6E-6
  |OR=.15
  |ORtxt=[0.084-0.212] unit increase
  |OA=1
}}

{{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}}