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rs3761547

From SNPedia

Orientationminus
Stabilizedminus
Make rs3761547(A;A)
Make rs3761547(A;G)
Make rs3761547(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position49262004
GeneFOXP3
is asnp
is mentioned by
dbSNPrs3761547
dbSNP (classic)rs3761547
ClinGenrs3761547
ebirs3761547
HLIrs3761547
Exacrs3761547
Gnomadrs3761547
Varsomers3761547
LitVarrs3761547
Maprs3761547
PheGenIrs3761547
Biobankrs3761547
1000 genomesrs3761547
hgdprs3761547
ensemblrs3761547
geneviewrs3761547
scholarrs3761547
googlers3761547
pharmgkbrs3761547
gwascentralrs3761547
openSNPrs3761547
23andMers3761547
SNPshotrs3761547
SNPdbers3761547
MSV3drs3761547
GWAS Ctlgrs3761547
GMAF0.1233
Max Magnitude0
? (A;A) (A;G) (G;G) 28


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


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

[PMID 17526924OA-icon.png] SNPs in the FOXP3 gene region show no association with Juvenile Idiopathic Arthritis in a UK Caucasian population.


[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].