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rs565186

From SNPedia

Orientationplus
Stabilizedplus
Make rs565186(C;C)
Make rs565186(C;T)
Make rs565186(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position101112898
GenePGR
is asnp
is mentioned by
dbSNPrs565186
ebirs565186
HLIrs565186
Exacrs565186
Varsomers565186
Maprs565186
PheGenIrs565186
hapmaprs565186
1000 genomesrs565186
hgdprs565186
ensemblrs565186
gopubmedrs565186
geneviewrs565186
scholarrs565186
googlers565186
pharmgkbrs565186
gwascentralrs565186
openSNPrs565186
23andMers565186
23andMe allrs565186
SNP Nexus

SNPshotrs565186
SNPdbers565186
MSV3drs565186
GWAS Ctlgrs565186
Max Magnitude
? (C;C) (C;T) (T;T) 28
Part of a haplotype Gs286, standalone effect for endometrial cancer is ambiguous. Tightly linked with PROGINS allele.
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 0.43
Odds Ratio 1.22 [1.00-1.50]

[PMID 15632380] Clarifying the PROGINS allele association in ovarian and breast cancer risk: a haplotype-based analysis