rs568157
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs568157(A;A) |
| Make rs568157(A;G) |
| Make rs568157(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 101153551 |
| Gene | PGR-AS1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs568157 |
| dbSNP (classic) | rs568157 |
| ClinGen | rs568157 |
| ebi | rs568157 |
| HLI | rs568157 |
| Exac | rs568157 |
| Gnomad | rs568157 |
| Varsome | rs568157 |
| LitVar | rs568157 |
| Map | rs568157 |
| PheGenI | rs568157 |
| Biobank | rs568157 |
| 1000 genomes | rs568157 |
| hgdp | rs568157 |
| ensembl | rs568157 |
| geneview | rs568157 |
| scholar | rs568157 |
| rs568157 | |
| pharmgkb | rs568157 |
| gwascentral | rs568157 |
| openSNP | rs568157 |
| 23andMe | rs568157 |
| SNPshot | rs568157 |
| SNPdbe | rs568157 |
| MSV3d | rs568157 |
| GWAS Ctlg | rs568157 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
Part of a haplotype Gs286, standalone effect for endometrial cancer is ambiguous.
No statistically significant interaction with 17-alpha-hydroxyprogesterone caproate for reducing recurrent preterm birth detected. [PMID 21600550
]
| 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 | 0.47 |
| Odds Ratio | 0.95 [0.82-1.11] |
[PMID 21600550
] Progesterone receptor polymorphisms and clinical response to 17-alpha-hydroxyprogesterone caproate
[PMID 15632380] Clarifying the PROGINS allele association in ovarian and breast cancer risk: a haplotype-based analysis
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 11
- Has genotype
- Has population
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip Ancestry v2
- On chip FTDNA2
- On chip FTDNA
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip NatGeo2
- On chip 23andMe v5
- On chip Ancestry v2c
- On chip Ancestry v2d
