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