rs1042838, PGR

N. diseases: 12
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
ovarian neoplasm
CUI: C0919267
Disease: ovarian neoplasm
0.030 GeneticVariation BEFREE This meta-analysis suggests that the two polymorphisms of PGR, Alu insertion and Val660Leu, may contribute to ovarian cancer susceptibility as low-penetrance risk factors. 25228088 2015
ovarian neoplasm
CUI: C0919267
Disease: ovarian neoplasm
0.030 GeneticVariation BEFREE Five haplotypes occurred with greater than 5% frequency, and the haplotype carrying the V</span>660L variant had a significant association with ovarian cancer (odds ratio = 0.76, 95% confidence interval: 0.62, 0.92). 15718480 2005
ovarian neoplasm
CUI: C0919267
Disease: ovarian neoplasm
0.030 GeneticVariation BEFREE No significant association between progesterone receptor exon 4 Val660Leu G/T polymorphism and risk of ovarian cancer. 11323389 2001