rs499590
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs499590(A;A) |
| Make rs499590(A;G) |
| Make rs499590(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 101143195 |
| Gene | PGR-AS1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs499590 |
| dbSNP (classic) | rs499590 |
| ClinGen | rs499590 |
| ebi | rs499590 |
| HLI | rs499590 |
| Exac | rs499590 |
| Gnomad | rs499590 |
| Varsome | rs499590 |
| LitVar | rs499590 |
| Map | rs499590 |
| PheGenI | rs499590 |
| Biobank | rs499590 |
| 1000 genomes | rs499590 |
| hgdp | rs499590 |
| ensembl | rs499590 |
| geneview | rs499590 |
| scholar | rs499590 |
| rs499590 | |
| pharmgkb | rs499590 |
| gwascentral | rs499590 |
| openSNP | rs499590 |
| 23andMe | rs499590 |
| SNPshot | rs499590 |
| SNPdbe | rs499590 |
| MSV3d | rs499590 |
| GWAS Ctlg | rs499590 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
Part of a haplotype, standalone effect is ambiguous.
| GWAS snp | |
|---|---|
| PMID | [PMID 20547493 ]
|
| Trait | Ovarian cancer |
| Title | Genetic variation in the progesterone receptor gene and risk of endometrial cancer: a haplotype-based approach. |
| Risk Allele | C |
| P-val | 0.010 |
| Odds Ratio | 0.95 [0.81-1.12] |
