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rs481775

From SNPedia

Orientationplus
Stabilizedplus
Make rs481775(A;A)
Make rs481775(A;G)
Make rs481775(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position101123944
GenePGR
is asnp
is mentioned by
dbSNPrs481775
ebirs481775
HLIrs481775
Exacrs481775
Varsomers481775
Maprs481775
PheGenIrs481775
hapmaprs481775
1000 genomesrs481775
hgdprs481775
ensemblrs481775
gopubmedrs481775
geneviewrs481775
scholarrs481775
googlers481775
pharmgkbrs481775
gwascentralrs481775
openSNPrs481775
23andMers481775
23andMe allrs481775
SNP Nexus

SNPshotrs481775
SNPdbers481775
MSV3drs481775
GWAS Ctlgrs481775
Max Magnitude
Part of a haplotype Gs286, standalone effect for endometrial cancer is ambiguous. p-values account for ethnic heterogenity of study population.

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.

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

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 A
P-val 0.86
Odds Ratio 0.84 [0.71-0.99]