{{Rsnum
|rsid=3761548
|Gene=FOXP3
|Chromosome=X
|position=49261784
|Orientation=minus
|GMAF=0.2727
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene_s=FOXP3
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 24.6 | 24.6 | 50.8
| HCB | 8.9 | 20.0 | 71.1
| JPT | 13.6 | 6.8 | 79.5
| YRI | 2.8 | 3.4 | 93.8
| ASW | 3.6 | 1.8 | 94.6
| CHB | 8.9 | 20.0 | 71.1
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 3.7 | 1.9 | 94.4
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{PMID Auto
|PMID=19679154
|Title=Genetic association study of FOXP3 polymorphisms in allergic rhinitis in Chinese population
}}

{{PMID Auto
|PMID=20414968
|Title=Intron-1 rs3761548 is related to the defective transcription of Foxp3 in psoriasis through abrogating E47/c-Myb binding
}}

{{PMID Auto
|PMID=21481380
|Title=Analysis of FOXP3 polymorphisms in infertile women with and without endometriosis
}}

{{PMID Auto
|PMID=21876709
|Title=Association between functional polymorphisms of Foxp3 gene and the occurrence of unexplained recurrent spontaneous abortion in a Chinese Han population
|OA=1
}}

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

{{PMID Auto
|PMID=22435141
|Title=An association study of single nucleotide polymorphisms of the FOXP3 intron-1 and the risk of Psoriasis vulgaris.
}}

{{PMID|18505474}} Retraction. Intron-1 rs3761548 is related to the defective transcription of Foxp3 in psoriasis through abrogating E47/c-Myb binding.

{{PMID|19141582|OA=1
}} Autoimmune thyroiditis and diabetes: dissecting the joint genetic susceptibility in a large cohort of multiplex families.

{{PMID|19145706}} Notice of retraction: "Intron-1 rs3761548 is related to the defective transcription of Foxp3 in psoriasis through abrogating E47/c-Myb binding".

{{PMID|19956101|OA=1
}} Overview of the Rapid Response data.

{{PMID|19956106|OA=1
}} Analysis of 19 genes for association with type I diabetes in the Type I Diabetes Genetics Consortium families.

{{PMID|20028375}} X-chromosome Forkhead Box P3 polymorphisms associate with atopy in girls in three Dutch birth cohorts.

{{PMID|21763379}} The rs3761548 polymorphism of FOXP3 is a protective genetic factor against allergic rhinitis in the Hungarian female population.

{{PMID Auto
|PMID=23450493
|Title=[Association of FOXP3 gene polymorphism in Chinese women with endometriosis]
}}

{{PMID Auto
|PMID=24035934
|Title=FoxP3 genetic variants and risk of non-small cell lung cancer in the Chinese Han population
}}

{{PMID Auto
|PMID=23498308
|Title=Association of FOXP3 (rs3761548) promoter polymorphism with nondermatomal vitiligo: A study from India
}}

{{PMID Auto
|PMID=23562195
|Title=Some polymorphisms in Epstein-Barr virus-induced gene 3 modify the risk for chronic rhinosinusitis
}}

{{PMID Auto
|PMID=22809231
|Title=Role of Foxp3 gene in maternal susceptibility to pre-eclampsia - a study from South India.
}}

{{PMID Auto
|PMID=22836044
|Title=Association between polymorphisms in FOXP3 and EBI3 genes and the risk for development of allergic rhinitis in Chinese subjects.
}}

{{PMID Auto
|PMID=23299803
|Title=FOXP3 genetic variant and risk of acute coronary syndrome in Chinese Han population.
}}

{{PMID Auto
|PMID=23582052
|Title=Association between FOXP3 polymorphisms and vitiligo in a Han Chinese population.
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Illumina Human 1M}}