rs529359

Orientation

minus

Stabilized

minus

Make rs529359(A;A)

Make rs529359(A;G)

Make rs529359(G;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

101123115

Gene

PGR

is a	snp
is	mentioned by
dbSNP	rs529359
dbSNP (classic)	rs529359
ClinGen	rs529359
ebi	rs529359
HLI	rs529359
Exac	rs529359
Gnomad	rs529359
Varsome	rs529359
LitVar	rs529359
Map	rs529359
PheGenI	rs529359
Biobank	rs529359
1000 genomes	rs529359
hgdp	rs529359
ensembl	rs529359
geneview	rs529359
scholar	rs529359
google	rs529359
pharmgkb	rs529359
gwascentral	rs529359
openSNP	rs529359
23andMe	rs529359
SNPshot	rs529359
SNPdbe	rs529359
MSV3d	rs529359
GWAS Ctlg	rs529359

Max Magnitude

0

?	(A;A) (A;G) (G;G)	28

Part of a haplotype Gs286, standalone effect for endometrial cancer is ambiguous.

In [PMID 20148360], no evidence for linkage to colorectal cancer in women was found in a study with 158 European subjects and 563 controls.

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	0.031
Odds Ratio	1.03 [0.89-1.2]

[PMID 20148360] Genetic variation in sex-steroid receptors and synthesizing enzymes and colorectal cancer risk in women.

[PMID 12560875] Catalog of 668 SNPs detected among 31 genes encoding potential drug targets on the cell surface

[Epidemiologic Study of Genetic Variation in Hormonal Pathways in Relation to the Effect of Hormone Replacement Therapy on Breast Cancer Risk]