rs481775
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs481775(A;A) |
Make rs481775(A;G) |
Make rs481775(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 101123944 |
Gene | PGR |
is a | snp |
is | mentioned by |
dbSNP | rs481775 |
dbSNP (classic) | rs481775 |
ClinGen | rs481775 |
ebi | rs481775 |
HLI | rs481775 |
Exac | rs481775 |
Gnomad | rs481775 |
Varsome | rs481775 |
LitVar | rs481775 |
Map | rs481775 |
PheGenI | rs481775 |
Biobank | rs481775 |
1000 genomes | rs481775 |
hgdp | rs481775 |
ensembl | rs481775 |
geneview | rs481775 |
scholar | rs481775 |
rs481775 | |
pharmgkb | rs481775 |
gwascentral | rs481775 |
openSNP | rs481775 |
23andMe | rs481775 |
SNPshot | rs481775 |
SNPdbe | rs481775 |
MSV3d | rs481775 |
GWAS Ctlg | rs481775 |
Max Magnitude | 0 |
Part of a haplotype Gs286, standalone effect for endometrial cancer is ambiguous. p-values account for ethnic heterogenity of study population.
In [PMID 20148360], no evidence for linkage to colorectal cancer in women was found in a study with 158 European subjects and 563 controls.
[PMID 20148360] Genetic variation in sex-steroid receptors and synthesizing enzymes and colorectal cancer risk in women.
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 | A |
P-val | 0.86 |
Odds Ratio | 0.84 [0.71-0.99] |