rs590688
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs590688(C;C) |
| Make rs590688(C;G) |
| Make rs590688(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 101105243 |
| Gene | PGR |
| is a | snp |
| is | mentioned by |
| dbSNP | rs590688 |
| dbSNP (classic) | rs590688 |
| ClinGen | rs590688 |
| ebi | rs590688 |
| HLI | rs590688 |
| Exac | rs590688 |
| Gnomad | rs590688 |
| Varsome | rs590688 |
| LitVar | rs590688 |
| Map | rs590688 |
| PheGenI | rs590688 |
| Biobank | rs590688 |
| 1000 genomes | rs590688 |
| hgdp | rs590688 |
| ensembl | rs590688 |
| geneview | rs590688 |
| scholar | rs590688 |
| rs590688 | |
| pharmgkb | rs590688 |
| gwascentral | rs590688 |
| openSNP | rs590688 |
| 23andMe | rs590688 |
| SNPshot | rs590688 |
| SNPdbe | rs590688 |
| MSV3d | rs590688 |
| GWAS Ctlg | rs590688 |
| GMAF | 0.4013 |
| Max Magnitude | 0 |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 21086036
] Association of progesterone receptor polymorphism with idiopathic recurrent pregnancy loss in Taiwanese Han population
[PMID 23764995] Association of progesterone receptor gene (PGR) variants and breast cancer risk in African American women.
