Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10069690
rs10069690
0.710 GeneticVariation BEFREE A splicing variant in TERT, rs10069690, showed a statistically significant interaction with ET use for risk of serous ovarian cancer (p<sub>int</sub>  = 0.013). 27420401

2016

dbSNP: rs10069690
rs10069690
T 0.710 GeneticVariation GWASCAT Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer. 28346442

2017

dbSNP: rs10088218
rs10088218
0.710 GeneticVariation BEFREE To assess the potential implications of microRNAs in ovarian cancer, we investigated the associations between microRNA expression and seven ovarian cancer risk variants discovered from genome-wide association studies (GWAS), namely, rs3814113 on 9p22.2, rs2072590 on 2q31, rs2665390 on 3q25, rs10088218, rs1516982, rs10098821 on 8q24.21 and rs2363956 on 19p13. 22235027

2012

dbSNP: rs10088218
rs10088218
0.710 GeneticVariation GWASCAT GWAS meta-analysis and replication identifies three new susceptibility loci for ovarian cancer. 23535730

2013

dbSNP: rs10088218
rs10088218
G 0.710 GeneticVariation GWASCAT A genome-wide association study identifies susceptibility loci for ovarian cancer at 2q31 and 8q24. 20852632

2010

dbSNP: rs10098821
rs10098821
0.010 GeneticVariation BEFREE To assess the potential implications of microRNAs in ovarian cancer, we investigated the associations between microRNA expression and seven ovarian cancer risk variants discovered from genome-wide association studies (GWAS), namely, rs3814113 on 9p22.2, rs2072590 on 2q31, rs2665390 on 3q25, rs10088218, rs1516982, rs10098821 on 8q24.21 and rs2363956 on 19p13. 22235027

2012

dbSNP: rs1011970
rs1011970
T 0.700 GeneticVariation GWASCAT Cross-Cancer Genome-Wide Analysis of Lung, Ovary, Breast, Prostate, and Colorectal Cancer Reveals Novel Pleiotropic Associations. 27197191

2016

dbSNP: rs1024611
rs1024611
0.010 GeneticVariation BEFREE These data suggest that MCP-1 rs1024611A/G and rs3760396C/G polymorphisms are associated with increased susceptibility to ovarian cancer, in which rs1024611A/G may increase serum level of MCP-1 in the Chinese population. 25289731

2015

dbSNP: rs10260419
rs10260419
0.700 GeneticVariation GWASCAT Genome-wide association studies identify susceptibility loci for epithelial ovarian cancer in east Asian women. 30898391

2019

dbSNP: rs1042522
rs1042522
0.040 GeneticVariation BEFREE Cumulative risk analysis revealed 3 unfavorable variants that increased significantly the risk of developing ovarian cancer (p.Ile1145 = ABCB1+ p.Asp1853Asn ATM+ p.Ser406Ala ATP7B- OR 7,47; p = 0,002) and significantly modified the progression free survival (PFS) of the patients, and also two favorable genotypes which protected against ovarian cancer (p.Arg952Lys ATP7B+ p.Arg72Pro TP53- OR 0,50; p = 0,008). 25591549

2015

dbSNP: rs1042522
rs1042522
0.040 GeneticVariation BEFREE The rs1042522 polymorphism was not overall associated with o</span>varian cancer risk. 25060098

2014

dbSNP: rs1042522
rs1042522
0.040 GeneticVariation BEFREE In conclusion SNPs in WRAP53 (rs2287497 and rs2287498) have stronger association with an ovarian cancer risk than rs1042522 in TP53. 23192612

2013

dbSNP: rs1042522
rs1042522
0.040 GeneticVariation BEFREE Meta-analysis shows significant association of the TP53 Arg72Pro with ovarian cancer risk. 21952824

2012

dbSNP: rs1042838
rs1042838
PGR
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

dbSNP: rs1042838
rs1042838
PGR
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

dbSNP: rs1042838
rs1042838
PGR
0.030 GeneticVariation BEFREE No significant association between progesterone receptor exon 4 Val660Leu G/T polymorphism and risk of ovarian cancer. 11323389

2001

dbSNP: rs1045485
rs1045485
0.020 GeneticVariation BEFREE In the present study we investigate the relevance of RAD51 -135C > G, TP53 R72P, NQO1*2 and CASP8 D302H polymorphisms as potential modifiers of BC and/or OC susceptibility conferred by these mutations. 19214744

2010

dbSNP: rs1045485
rs1045485
0.020 GeneticVariation BEFREE The minor allele of CASP8 D302H was significantly associated with a reduced risk of breast cancer (per-allele HR, 0.85; 95% CI, 0.76-0.97; P(trend) = 0.011) and ovarian cancer (per-allele HR, 0.69; 95% CI, 0.53-0.89; P(trend) = 0.004) for BRCA1 but not for BRCA2 mutation carriers. 20978178

2010

dbSNP: rs1046428
rs1046428
0.010 GeneticVariation BEFREE We genotyped GSTA2_448_C > G (rs2180314), GSTA2_742_A > C (rs6577), GSTM2_-832_T > C (rs638820), GSTO1_-1242_G > A (rs2164624), GSTO1_419_A > C (rs4925), GSTO2_-183_A > G (rs2297235), GSTO2_342_A > G (rs156697), GSTZ1_-4378_A > G (rs1046428), and GSTZ1_94_G > A (rs3177427) by MALDI-TOF MS in the German GENICA breast cancer case-control collection of 1021 cases and 1015 controls and performed breast cancer risk association in general and with respect to the stratifications: menopausal status, family history of breast or ovarian cancer, use of oral contraceptives, use of hormone therapy, body mass index, and smoking as well as histopathological tumor characteristics including hormone receptor status, grade, histology, and node status. 19859803

2010

dbSNP: rs104886003
rs104886003
A 0.710 CausalMutation CLINVAR PI3K/AKT/mTOR inhibitors in patients with breast and gynecologic malignancies harboring PIK3CA mutations. 22271473

2012

dbSNP: rs104886003
rs104886003
A 0.710 GeneticVariation CLINVAR

dbSNP: rs104886003
rs104886003
A 0.710 CausalMutation CLINVAR Phosphatidylinositol 3-kinase mutations identified in human cancer are oncogenic. 15647370

2005

dbSNP: rs104886003
rs104886003
0.710 GeneticVariation BEFREE We also found that an activating (E545K) Pik3ca mutation, unlike Pten inactivation or Pik3ca H1047R mutation, cannot cooperate with Arid1a loss to promote ovarian cancer development in the mouse. 26279473

2016

dbSNP: rs1048943
rs1048943
0.030 GeneticVariation BEFREE Ile462Val status seems to represent a meaningful risk factor for ovarian cancer in Caucasians. 22733497

2012

dbSNP: rs1048943
rs1048943
0.030 GeneticVariation BEFREE CYP1A1 Ile462Val is a risk factor for ovarian cancer development. 22277800

2012