rs1870019
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1870019(C;C) |
| Make rs1870019(C;T) |
| Make rs1870019(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 11 |
| Position | 101030742 |
| Gene | PGR |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1870019 |
| dbSNP (classic) | rs1870019 |
| ClinGen | rs1870019 |
| ebi | rs1870019 |
| HLI | rs1870019 |
| Exac | rs1870019 |
| Gnomad | rs1870019 |
| Varsome | rs1870019 |
| LitVar | rs1870019 |
| Map | rs1870019 |
| PheGenI | rs1870019 |
| Biobank | rs1870019 |
| 1000 genomes | rs1870019 |
| hgdp | rs1870019 |
| ensembl | rs1870019 |
| geneview | rs1870019 |
| scholar | rs1870019 |
| rs1870019 | |
| pharmgkb | rs1870019 |
| gwascentral | rs1870019 |
| openSNP | rs1870019 |
| 23andMe | rs1870019 |
| SNPshot | rs1870019 |
| SNPdbe | rs1870019 |
| MSV3d | rs1870019 |
| GWAS Ctlg | rs1870019 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
Part of a haplotype Gs286, standalone effect for endometrial cancer and ovarian cancer is ambiguous. p-values account for ethnic heterogenity of study population.
| 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 | 0.74 |
| Odds Ratio | 0.91 [0.77-1.08] |
[PMID 15632380] Clarifying the PROGINS allele association in ovarian and breast cancer risk: a haplotype-based analysis
