rs590688
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs590688(C;C) |
Make rs590688(C;G) |
Make rs590688(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 101105243 |
Gene | PGR |
is a | snp |
is | mentioned by |
dbSNP | rs590688 |
dbSNP (classic) | rs590688 |
ClinGen | rs590688 |
ebi | rs590688 |
HLI | rs590688 |
Exac | rs590688 |
Gnomad | rs590688 |
Varsome | rs590688 |
LitVar | rs590688 |
Map | rs590688 |
PheGenI | rs590688 |
Biobank | rs590688 |
1000 genomes | rs590688 |
hgdp | rs590688 |
ensembl | rs590688 |
geneview | rs590688 |
scholar | rs590688 |
rs590688 | |
pharmgkb | rs590688 |
gwascentral | rs590688 |
openSNP | rs590688 |
23andMe | rs590688 |
SNPshot | rs590688 |
SNPdbe | rs590688 |
MSV3d | rs590688 |
GWAS Ctlg | rs590688 |
GMAF | 0.4013 |
Max Magnitude | 0 |
? | (C;C) (C;G) (G;G) | 28 |
---|---|---|
|
[PMID 21086036] Association of progesterone receptor polymorphism with idiopathic recurrent pregnancy loss in Taiwanese Han population
[PMID 23764995] Association of progesterone receptor gene (PGR) variants and breast cancer risk in African American women.