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rs608995

From SNPedia

Orientationplus
Stabilizedplus
Make rs608995(A;A)
Make rs608995(A;T)
Make rs608995(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position101035002
GenePGR
is asnp
is mentioned by
dbSNPrs608995
ebirs608995
HLIrs608995
Exacrs608995
Varsomers608995
Maprs608995
PheGenIrs608995
hapmaprs608995
1000 genomesrs608995
hgdprs608995
ensemblrs608995
gopubmedrs608995
geneviewrs608995
scholarrs608995
googlers608995
pharmgkbrs608995
gwascentralrs608995
openSNPrs608995
23andMers608995
23andMe allrs608995
SNP Nexus

SNPshotrs608995
SNPdbers608995
MSV3drs608995
GWAS Ctlgrs608995
GMAF0.2824
Max Magnitude
[PMID 15632380] Two SNPs in block 4 were associated with an increased risk of ovarian cancer among homozygous carriers as compared with noncarriers: rs1042838 (PROGINS allele; odds ratio [OR] = 3.23, 95% confidence interval [CI] = 1.19 to 8.75, P = .022) and rs608995 (minor allele; OR = 3.10, 95% CI = 1.63 to 5.89, P<.001)


[PMID 20547493OA-icon.png] Genetic variation in the progesterone receptor gene and risk of endometrial cancer: a haplotype-based approach


[PMID 22121098] Worldwide distribution of allelic variation at the progesterone receptor locus and the incidence of female reproductive cancers

[PMID 18219286OA-icon.png] Progesterone receptor variation and risk of ovarian cancer is limited to the invasive endometrioid subtype: results from the Ovarian Cancer Association Consortium pooled analysis.