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rs590688

From SNPedia

Orientationplus
Stabilizedplus
Make rs590688(C;C)
Make rs590688(C;G)
Make rs590688(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position101105243
GenePGR
is asnp
is mentioned by
dbSNPrs590688
ebirs590688
HLIrs590688
Exacrs590688
Varsomers590688
Maprs590688
PheGenIrs590688
hapmaprs590688
1000 genomesrs590688
hgdprs590688
ensemblrs590688
gopubmedrs590688
geneviewrs590688
scholarrs590688
googlers590688
pharmgkbrs590688
gwascentralrs590688
openSNPrs590688
23andMers590688
23andMe allrs590688
SNP Nexus

SNPshotrs590688
SNPdbers590688
MSV3drs590688
GWAS Ctlgrs590688
GMAF0.4013
Max Magnitude
? (C;C) (C;G) (G;G) 28
[PMID 21086036OA-icon.png] Association of progesterone receptor polymorphism with idiopathic recurrent pregnancy loss in Taiwanese Han population


[PMID 23764995OA-icon.png] Association of progesterone receptor gene (PGR) variants and breast cancer risk in African American women.