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].
