rs565186
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs565186(C;C) |
Make rs565186(C;T) |
Make rs565186(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 101112898 |
Gene | PGR |
is a | snp |
is | mentioned by |
dbSNP | rs565186 |
dbSNP (classic) | rs565186 |
ClinGen | rs565186 |
ebi | rs565186 |
HLI | rs565186 |
Exac | rs565186 |
Gnomad | rs565186 |
Varsome | rs565186 |
LitVar | rs565186 |
Map | rs565186 |
PheGenI | rs565186 |
Biobank | rs565186 |
1000 genomes | rs565186 |
hgdp | rs565186 |
ensembl | rs565186 |
geneview | rs565186 |
scholar | rs565186 |
rs565186 | |
pharmgkb | rs565186 |
gwascentral | rs565186 |
openSNP | rs565186 |
23andMe | rs565186 |
SNPshot | rs565186 |
SNPdbe | rs565186 |
MSV3d | rs565186 |
GWAS Ctlg | rs565186 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
Part of a haplotype Gs286, standalone effect for endometrial cancer is ambiguous. Tightly linked with PROGINS allele.
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 | C |
P-val | 0.43 |
Odds Ratio | 1.22 [1.00-1.50] |
[PMID 15632380] Clarifying the PROGINS allele association in ovarian and breast cancer risk: a haplotype-based analysis