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rs660541

From SNPedia

Orientationplus
Stabilizedplus
Make rs660541(A;A)
Make rs660541(A;G)
Make rs660541(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position101063636
GenePGR
is asnp
is mentioned by
dbSNPrs660541
ebirs660541
HLIrs660541
Exacrs660541
Varsomers660541
Maprs660541
PheGenIrs660541
hapmaprs660541
1000 genomesrs660541
hgdprs660541
ensemblrs660541
gopubmedrs660541
geneviewrs660541
scholarrs660541
googlers660541
pharmgkbrs660541
gwascentralrs660541
openSNPrs660541
23andMers660541
23andMe allrs660541
SNP Nexus

SNPshotrs660541
SNPdbers660541
MSV3drs660541
GWAS Ctlgrs660541
Max Magnitude
? (A;A) (A;G) (G;G) 28
Part of a haplotype Gs286, standalone effect for endometrial cancer is ambiguous.
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 G
P-val 0.31
Odds Ratio 1.06 [0.92-1.22]

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