rs660541
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs660541(A;A) |
| Make rs660541(A;G) |
| Make rs660541(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 101063636 |
| Gene | PGR |
| is a | snp |
| is | mentioned by |
| dbSNP | rs660541 |
| dbSNP (classic) | rs660541 |
| ClinGen | rs660541 |
| ebi | rs660541 |
| HLI | rs660541 |
| Exac | rs660541 |
| Gnomad | rs660541 |
| Varsome | rs660541 |
| LitVar | rs660541 |
| Map | rs660541 |
| PheGenI | rs660541 |
| Biobank | rs660541 |
| 1000 genomes | rs660541 |
| hgdp | rs660541 |
| ensembl | rs660541 |
| geneview | rs660541 |
| scholar | rs660541 |
| rs660541 | |
| pharmgkb | rs660541 |
| gwascentral | rs660541 |
| openSNP | rs660541 |
| 23andMe | rs660541 |
| SNPshot | rs660541 |
| SNPdbe | rs660541 |
| MSV3d | rs660541 |
| GWAS Ctlg | rs660541 |
| 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 | G |
| P-val | 0.31 |
| Odds Ratio | 1.06 [0.92-1.22] |
[PMID 15632380] Clarifying the PROGINS allele association in ovarian and breast cancer risk: a haplotype-based analysis
