rs3761547
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs3761547(A;A) |
Make rs3761547(A;G) |
Make rs3761547(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | X |
Position | 49262004 |
Gene | FOXP3 |
is a | snp |
is | mentioned by |
dbSNP | rs3761547 |
dbSNP (classic) | rs3761547 |
ClinGen | rs3761547 |
ebi | rs3761547 |
HLI | rs3761547 |
Exac | rs3761547 |
Gnomad | rs3761547 |
Varsome | rs3761547 |
LitVar | rs3761547 |
Map | rs3761547 |
PheGenI | rs3761547 |
Biobank | rs3761547 |
1000 genomes | rs3761547 |
hgdp | rs3761547 |
ensembl | rs3761547 |
geneview | rs3761547 |
scholar | rs3761547 |
rs3761547 | |
pharmgkb | rs3761547 |
gwascentral | rs3761547 |
openSNP | rs3761547 |
23andMe | rs3761547 |
SNPshot | rs3761547 |
SNPdbe | rs3761547 |
MSV3d | rs3761547 |
GWAS Ctlg | rs3761547 |
GMAF | 0.1233 |
Max Magnitude | 0 |
? | (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 17526924] 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].