rs5902434
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs5902434(-;-) |
| Make rs5902434(-;ATT) |
| Make rs5902434(ATT;ATT) |
| Reference | GRCh38 38.1/141 |
| Chromosome | X |
| Position | 49264512 |
| Gene | FOXP3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs5902434 |
| dbSNP (classic) | rs5902434 |
| ClinGen | rs5902434 |
| ebi | rs5902434 |
| HLI | rs5902434 |
| Exac | rs5902434 |
| Gnomad | rs5902434 |
| Varsome | rs5902434 |
| LitVar | rs5902434 |
| Map | rs5902434 |
| PheGenI | rs5902434 |
| Biobank | rs5902434 |
| 1000 genomes | rs5902434 |
| hgdp | rs5902434 |
| ensembl | rs5902434 |
| geneview | rs5902434 |
| scholar | rs5902434 |
| rs5902434 | |
| pharmgkb | rs5902434 |
| gwascentral | rs5902434 |
| openSNP | rs5902434 |
| 23andMe | rs5902434 |
| SNPshot | rs5902434 |
| SNPdbe | rs5902434 |
| MSV3d | rs5902434 |
| GWAS Ctlg | rs5902434 |
| Max Magnitude | 0 |
[PMID 21876709
] Association between functional polymorphisms of Foxp3 gene and the occurrence of unexplained recurrent spontaneous abortion in a Chinese Han population
[PMID 23560055] Foxp3 (-/ATT) Polymorphism Contributes to the Susceptibility of Preeclampsia
[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 30027704] Association of FOXP3 Single Nucleotide Polymorphisms With Clinical Outcomes After Allogenic Hematopoietic Stem Cell Transplantation.
