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rs3761548

From SNPedia

Orientationminus
Stabilizedminus
Make rs3761548(A;A)
Make rs3761548(A;C)
Make rs3761548(C;C)
ReferenceGRCh38 38.1/141
ChromosomeX
Position49261784
GeneFOXP3
is asnp
is mentioned by
dbSNPrs3761548
ebirs3761548
HLIrs3761548
Exacrs3761548
Varsomers3761548
Maprs3761548
PheGenIrs3761548
hapmaprs3761548
1000 genomesrs3761548
hgdprs3761548
ensemblrs3761548
gopubmedrs3761548
geneviewrs3761548
scholarrs3761548
googlers3761548
pharmgkbrs3761548
gwascentralrs3761548
openSNPrs3761548
23andMers3761548
23andMe allrs3761548
SNP Nexus

SNPshotrs3761548
SNPdbers3761548
MSV3drs3761548
GWAS Ctlgrs3761548
GMAF0.2727
Max Magnitude
? (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 21876709OA-icon.png] 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 19141582OA-icon.png] 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 19956101OA-icon.png] Overview of the Rapid Response data.

[PMID 19956106OA-icon.png] 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.