rs3761548
| Orientation | minus |
| Stabilized | minus |
| Make rs3761548(A;A) |
| Make rs3761548(A;C) |
| Make rs3761548(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | X |
| Position | 49261784 |
| Gene | FOXP3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3761548 |
| dbSNP (classic) | rs3761548 |
| ClinGen | rs3761548 |
| ebi | rs3761548 |
| HLI | rs3761548 |
| Exac | rs3761548 |
| Gnomad | rs3761548 |
| Varsome | rs3761548 |
| LitVar | rs3761548 |
| Map | rs3761548 |
| PheGenI | rs3761548 |
| Biobank | rs3761548 |
| 1000 genomes | rs3761548 |
| hgdp | rs3761548 |
| ensembl | rs3761548 |
| geneview | rs3761548 |
| scholar | rs3761548 |
| rs3761548 | |
| pharmgkb | rs3761548 |
| gwascentral | rs3761548 |
| openSNP | rs3761548 |
| 23andMe | rs3761548 |
| SNPshot | rs3761548 |
| SNPdbe | rs3761548 |
| MSV3d | rs3761548 |
| GWAS Ctlg | rs3761548 |
| GMAF | 0.2727 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
|
| ||
[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.
[PMID 26882813] A Single Nucleotide Polymorphism in the FOXP3 Gene Associated with Behçet's Disease in an Iranian Population.
[PMID 28253599] [Association of ulcerative colitis with fork head/winged helix transcription factor-3 gene polymorphisms in Chinese patients].
[PMID 28741671] The Impact of FOXP3 Polymorphism on the Risk of Allergic Rhinitis: A Meta-Analysis.
[PMID 30027704] Association of FOXP3 Single Nucleotide Polymorphisms With Clinical Outcomes After Allogenic Hematopoietic Stem Cell Transplantation.
[PMID 30057362] Serum concentration of interleukin-35 and its association with tumor stages and FOXP3 gene polymorphism in patients with prostate cancer.
[PMID 30168273] FOXP3 rs3761548 polymorphism is associated with knee osteoarthritis in a Turkish population.
[PMID 32377237] ASSOCIATION OF FOXP3 GENE VARIANTS WITH RISK OF HASHIMOTO'S THYROIDITIS AND CORRELATION WITH ANTI-TPO ANTIBODY LEVELS.
[PMID 33127257] Association of Foxp3 rs3761548 polymorphism with cytokines concentration in gastric adenocarcinoma patients.
[PMID 33444682] Gender Bias in the Genetic Vulnerability Towards Type 2 Diabetes and Diabetic nephropathy: Role of Forkhead Box Protein3 Transcription Factor Gene Variants.
