{{Rsnum
|rsid=3761547
|Gene=FOXP3
|Chromosome=X
|position=49262004
|Orientation=minus
|GMAF=0.1233
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=FOXP3
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 77.9 | 13.3 | 8.8
| HCB | 72.3 | 19.7 | 8.0
| JPT | 68.1 | 18.6 | 13.3
| YRI | 97.3 | 1.4 | 1.4
| ASW | 93.0 | 7.0 | 0.0
| CHB | 72.3 | 19.7 | 8.0
| CHD | 73.4 | 18.3 | 8.3
| GIH | 63.0 | 16.0 | 21.0
| LWK | 97.3 | 0.0 | 2.7
| MEX | 87.9 | 6.9 | 5.2
| MKK | 89.7 | 5.2 | 5.2
| TSI | 88.2 | 4.9 | 6.9
| HapMapRevision=28
}}
{{PMID Auto
|PMID=19679154
|Title=Genetic association study of FOXP3 polymorphisms in allergic rhinitis in Chinese population
}}

{{PMID Auto
|PMID=22239151
|Title=Genetic Association of FOXP3 Gene Polymorphisms with Allograft Rejection in Renal Transplant Patients
}}

{{PMID|17526924|OA=1
}} SNPs in the FOXP3 gene region show no association with Juvenile Idiopathic Arthritis in a UK Caucasian population.

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}