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rs529359

From SNPedia

Orientationminus
Stabilizedminus
Make rs529359(A;A)
Make rs529359(A;G)
Make rs529359(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position101123115
GenePGR
is asnp
is mentioned by
dbSNPrs529359
ebirs529359
HLIrs529359
Exacrs529359
Varsomers529359
Maprs529359
PheGenIrs529359
hapmaprs529359
1000 genomesrs529359
hgdprs529359
ensemblrs529359
gopubmedrs529359
geneviewrs529359
scholarrs529359
googlers529359
pharmgkbrs529359
gwascentralrs529359
openSNPrs529359
23andMers529359
23andMe allrs529359
SNP Nexus

SNPshotrs529359
SNPdbers529359
MSV3drs529359
GWAS Ctlgrs529359
Max Magnitude
? (A;A) (A;G) (G;G) 28
Part of a haplotype Gs286, standalone effect for endometrial cancer is ambiguous.

In [PMID 20148360OA-icon.png], 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 20547493OA-icon.png]
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 20148360OA-icon.png] 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]