rs613120
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs613120(C;C) |
| Make rs613120(C;T) |
| Make rs613120(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 101103547 |
| Gene | PGR |
| is a | snp |
| is | mentioned by |
| dbSNP | rs613120 |
| dbSNP (classic) | rs613120 |
| ClinGen | rs613120 |
| ebi | rs613120 |
| HLI | rs613120 |
| Exac | rs613120 |
| Gnomad | rs613120 |
| Varsome | rs613120 |
| LitVar | rs613120 |
| Map | rs613120 |
| PheGenI | rs613120 |
| Biobank | rs613120 |
| 1000 genomes | rs613120 |
| hgdp | rs613120 |
| ensembl | rs613120 |
| geneview | rs613120 |
| scholar | rs613120 |
| rs613120 | |
| pharmgkb | rs613120 |
| gwascentral | rs613120 |
| openSNP | rs613120 |
| 23andMe | rs613120 |
| SNPshot | rs613120 |
| SNPdbe | rs613120 |
| MSV3d | rs613120 |
| GWAS Ctlg | rs613120 |
| Max Magnitude | 0 |
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 | 0.52 |
| Odds Ratio | 1.05 [0.91-1.21] |
[PMID 15632380] Clarifying the PROGINS allele association in ovarian and breast cancer risk: a haplotype-based analysis
