rs516693
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs516693(A;A) |
| Make rs516693(A;G) |
| Make rs516693(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 101093012 |
| Gene | PGR |
| is a | snp |
| is | mentioned by |
| dbSNP | rs516693 |
| dbSNP (classic) | rs516693 |
| ClinGen | rs516693 |
| ebi | rs516693 |
| HLI | rs516693 |
| Exac | rs516693 |
| Gnomad | rs516693 |
| Varsome | rs516693 |
| LitVar | rs516693 |
| Map | rs516693 |
| PheGenI | rs516693 |
| Biobank | rs516693 |
| 1000 genomes | rs516693 |
| hgdp | rs516693 |
| ensembl | rs516693 |
| geneview | rs516693 |
| scholar | rs516693 |
| rs516693 | |
| pharmgkb | rs516693 |
| gwascentral | rs516693 |
| openSNP | rs516693 |
| 23andMe | rs516693 |
| SNPshot | rs516693 |
| SNPdbe | rs516693 |
| MSV3d | rs516693 |
| GWAS Ctlg | rs516693 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
Part of a haplotype Gs286, standalone effect for endometrial cancer is ambiguous.
| GWAS snp | |
|---|---|
| PMID | [PMID 20547493 ]
|
| Trait | Endometrial cancer |
| Title | Genetic variation in the progesterone receptor gene and risk of endometrial cancer: a haplotype-based approach. |
| Risk Allele | T |
| P-val | 0.16 |
| Odds Ratio | 1.15 [0.95-1.39] |
[PMID 15632380] Clarifying the PROGINS allele association in ovarian and breast cancer risk: a haplotype-based analysis
