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rs499590

From SNPedia

Orientationminus
Stabilizedminus
Make rs499590(A;A)
Make rs499590(A;G)
Make rs499590(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position101143195
GeneLOC101054525
is asnp
is mentioned by
dbSNPrs499590
ebirs499590
HLIrs499590
Exacrs499590
Varsomers499590
Maprs499590
PheGenIrs499590
hapmaprs499590
1000 genomesrs499590
hgdprs499590
ensemblrs499590
gopubmedrs499590
geneviewrs499590
scholarrs499590
googlers499590
pharmgkbrs499590
gwascentralrs499590
openSNPrs499590
23andMers499590
23andMe allrs499590
SNP Nexus

SNPshotrs499590
SNPdbers499590
MSV3drs499590
GWAS Ctlgrs499590
Max Magnitude
? (A;A) (A;G) (G;G) 28
Part of a haplotype, standalone effect is ambiguous.
GWAS snp
PMID [PMID 20547493OA-icon.png]
Trait Ovarian cancer
Title Genetic variation in the progesterone receptor gene and risk of endometrial cancer: a haplotype-based approach.
Risk Allele C
P-val 0.010
Odds Ratio 0.95 [0.81-1.12]