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rs516693

From SNPedia

Orientationminus
Stabilizedminus
Make rs516693(A;A)
Make rs516693(A;G)
Make rs516693(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position101093012
GenePGR
is asnp
is mentioned by
dbSNPrs516693
ebirs516693
HLIrs516693
Exacrs516693
Varsomers516693
Maprs516693
PheGenIrs516693
hapmaprs516693
1000 genomesrs516693
hgdprs516693
ensemblrs516693
gopubmedrs516693
geneviewrs516693
scholarrs516693
googlers516693
pharmgkbrs516693
gwascentralrs516693
openSNPrs516693
23andMers516693
23andMe allrs516693
SNP Nexus

SNPshotrs516693
SNPdbers516693
MSV3drs516693
GWAS Ctlgrs516693
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 T
P-val 0.16
Odds Ratio 1.15 [0.95-1.39]

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