[PMID 19679154] Genetic association study of FOXP3 polymorphisms in allergic rhinitis in Chinese population


[PMID 20414968] Intron-1 rs3761548 is related to the defective transcription of Foxp3 in psoriasis through abrogating E47/c-Myb binding


[PMID 21481380] Analysis of FOXP3 polymorphisms in infertile women with and without endometriosis


[PMID 21876709] Association between functional polymorphisms of Foxp3 gene and the occurrence of unexplained recurrent spontaneous abortion in a Chinese Han population


[PMID 22239151] Genetic Association of FOXP3 Gene Polymorphisms with Allograft Rejection in Renal Transplant Patients


[PMID 22435141] 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] 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] Overview of the Rapid Response data.

[PMID 19956106] 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 23450493] [Association of FOXP3 gene polymorphism in Chinese women with endometriosis]


[PMID 24035934] FoxP3 genetic variants and risk of non-small cell lung cancer in the Chinese Han population


[PMID 23498308] Association of FOXP3 (rs3761548) promoter polymorphism with nondermatomal vitiligo: A study from India


[PMID 23562195] Some polymorphisms in Epstein-Barr virus-induced gene 3 modify the risk for chronic rhinosinusitis


[PMID 22809231] Role of Foxp3 gene in maternal susceptibility to pre-eclampsia - a study from South India.


[PMID 22836044] Association between polymorphisms in FOXP3 and EBI3 genes and the risk for development of allergic rhinitis in Chinese subjects.


[PMID 23299803] FOXP3 genetic variant and risk of acute coronary syndrome in Chinese Han population.


[PMID 23582052] Association between FOXP3 polymorphisms and vitiligo in a Han Chinese population.


[PMID 25499308] The transcription factor Forkhead Box P3 gene variants affect idiopathic recurrent pregnancy loss


[PMID 26735609] Effect of FOXP3 polymorphism on the clinical outcomes after allogeneic hematopoietic stem cell transplantation in pediatric acute leukemia patients.

rs3761548

Parent Gene: FOXP3

Importance: 1
Less common allele: T = 24%
More common allele: G = 76%
My Genotype: Log In