Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs567534295
rs567534295
0.010 GeneticVariation BEFREE Analyses performed under logistic model, linear mixed model, and model incorporating correlations identified nine significant associations with three gynecologic diseases including four novel findings (rs79219469:C > T, LINC02183, P = 3.3 × 10<sup>-8</sup> and rs567534295:C > T, BRCA1, P = 3.1 × 10<sup>-8</sup> with OC, rs150806792:C > T, INS-IGF2, P = 4.9 × 10<sup>-8</sup> and rs140991990:A > G, SOX9, P = 3.3 × 10<sup>-8</sup> with UCC). 31488892

2020

dbSNP: rs12373237
rs12373237
0.010 GeneticVariation BEFREE The CC homozygous mutation of rs12373237 was highly correlated with the onset of ovarian cancer (OR=4.333, P=0.028). 31402958

2019

dbSNP: rs137853011
rs137853011
0.010 GeneticVariation BEFREE This karyotype phenotype was not observed in other tested tissues or in an ovarian cancer patient with a different homozygous missense mutation in <i>CHEK2</i> (c.1283C>T; p.Ser428Phe). 30858171

2019

dbSNP: rs200640585
rs200640585
0.010 GeneticVariation BEFREE PMS2 germline mutation c.943C>T (p.Arg315*)-induced Lynch syndrome-associated ovarian cancer. 31056861

2019

dbSNP: rs2516839
rs2516839
0.010 GeneticVariation BEFREE Taken together, our results suggest that the rs2516839 polymorphism in USF1 gene may associate with the efficacy and safety of paclitaxel-based chemotherapy and prognosis in the treatment of OC. 29322800

2019

dbSNP: rs2699887
rs2699887
0.010 GeneticVariation BEFREE Interaction between PIK3CA rs2699887 SNP and age, number of liveborn, tobacco, alcohol, a family history of ovarian cancer and other factors are associated with ovarian cancer risk. 31288947

2019

dbSNP: rs3212986
rs3212986
0.010 GeneticVariation BEFREE ERCC1 rs3212986 (C/A) polymorphisms posed an increased risk for breast and ovarian cancer as whole (A vs C: OR = 1.12, 95% CI = 1.01-1.25; AA + CA vs CC: OR = 1.11, 95% CI = 1.02-1.22), and presented especially higher risk for ovarian cancer (A vs C: OR = 1.31, 95% CI = 1.05-1.63; AA vs CA + CC: OR = 1.66, 95% CI = 1.12-2.47; AA vs CC: OR = 1.72, 95% CI = 1.12-2.64). 31081240

2019

dbSNP: rs3737787
rs3737787
0.010 GeneticVariation BEFREE This study was supposed to investigate the correlation between the functional single nucleotide polymorphisms (SNPs) (rs2516839 and rs3737787) in USF1 gene and the efficacy and safety of paclitaxel-based chemotherapy and prognosis in the treatment of ovarian cancer (OC). 29322800

2019

dbSNP: rs3976507
rs3976507
0.010 GeneticVariation BEFREE Interaction between PIK3CA rs3976507 and rs6443626 loci, and factors such as BMI, number of liveborn, tobacco, alcohol, and family history of ovarian cancer are associated with ovarian cancer risk. 31288947

2019

dbSNP: rs587778617
rs587778617
0.010 GeneticVariation BEFREE PMS2 germline mutation c.943C>T (p.Arg315*)-induced Lynch syndrome-associated ovarian cancer. 31056861

2019

dbSNP: rs6443626
rs6443626
0.010 GeneticVariation BEFREE Interaction between PIK3CA rs3976507 and rs6443626 loci, and factors such as BMI, number of liveborn, tobacco, alcohol, and family history of ovarian cancer are associated with ovarian cancer risk. 31288947

2019

dbSNP: rs79722116
rs79722116
0.010 GeneticVariation BEFREE Additionally, two non-synonymous SNPs rs201407189 (c.973G>A, p.A325T) and rs1800367 (c.1345G>A, p.V449M), and two synonymous SNPs rs55719336 (c.816C>T, p.I272I) and rs79722116 (c.1407G>A, p.T469T) were identified in FBOC patients. 30967997

2019

dbSNP: rs80356897
rs80356897
0.010 GeneticVariation BEFREE Additionally, two non-synonymous SNPs rs201407189 (c.973G>A, p.A325T) and rs1800367 (c.1345G>A, p.V449M), and two synonymous SNPs rs55719336 (c.816C>T, p.I272I) and rs79722116 (c.1407G>A, p.T469T) were identified in FBOC patients. 30967997

2019

dbSNP: rs80357268
rs80357268
0.010 GeneticVariation BEFREE BRCA1, p.(Val1833Met) is possibly a disease-associated variant, supported by a likelihood ratio of 1.88, while a correlation to ovarian cancer is suspected. 31447071

2019

dbSNP: rs1136905
rs1136905
0.010 GeneticVariation BEFREE We established that <i>TP53</i> "hotspot" mutations (c.659A>G; p.Y220C and c.733G>A; p.G245S) expressed by two different patients' tumors were both immunogenic in the context of HLA-DRB3*02:02.<b>Conclusions:</b> Mutation-reactive T cells infiltrated ovarian cancer metastases at sufficient frequencies to warrant their investigation as adoptive cell therapy. 29853601

2018

dbSNP: rs1544410
rs1544410
VDR
0.010 GeneticVariation BEFREE Moreover, for detecting clinical risk of OC, heterozygote models with the rs1544410 (BsmI) polymorphism is likely the best genetic model for detecting the risk of OC in Caucasian patients. 30059751

2018

dbSNP: rs1801200
rs1801200
0.010 GeneticVariation BEFREE Furthermore, no significant association between allelic, dominant, codominant and recessive models of HER2 rs1801200 (V655I) and ovarian cancer was found (<i>p</i> > 0.05). 29535531

2018

dbSNP: rs1836724
rs1836724
0.010 GeneticVariation BEFREE The data indicated that the ERBB4 rs1836724 polymorphism was associated with the survival of ovarian cancer. 29125883

2018

dbSNP: rs186724
rs186724
0.010 GeneticVariation BEFREE Firstly, individuals carried ERBB4 rs186724 GG genotype had poorer overall survival compared with those carried CC/CT genotypes in ovarian cancer, while the participants with rs1836724 GA genotype had the same overall survival with that in participants with rs1836724 AA genotype in accordance with the result of Cox regression and Kaplan-Meier analyses. 29125883

2018

dbSNP: rs1899663
rs1899663
0.010 GeneticVariation BEFREE HOTAIR rs4759314 increased susceptibility to BC, CC, and OC in some patients; rs029778 and rs1899663 also increased susceptibility to some extent. 30484890

2018

dbSNP: rs1989839
rs1989839
0.010 GeneticVariation BEFREE CONCLUSIONS Polymorphisms of the RASSF1A gene, most significantly the CT genotype of rs1989839, might play a role in the development and prognosis of ovarian cancer in women in Southern China. 29670073

2018

dbSNP: rs2227982
rs2227982
0.010 GeneticVariation BEFREE PD-1 rs2227982 C>T and PD-L1 rs4143815 C>G polymorphisms increased the risk for ovarian cancer</span>. 29171986

2018

dbSNP: rs4143815
rs4143815
0.010 GeneticVariation BEFREE PD-1 rs2227982 C>T and PD-L1 rs4143815 C>G polymorphisms increased the risk for ovarian cancer. 29171986

2018

dbSNP: rs4759314
rs4759314
0.010 GeneticVariation BEFREE HOTAIR rs4759314 increased susceptibility to BC, CC, and OC in some patients; rs029778 and rs1899663 also increased susceptibility to some extent. 30484890

2018

dbSNP: rs671
rs671
0.010 GeneticVariation BEFREE Because the rs671 Lys allele causes ALDH2 inactivation leading to increased acetaldehyde exposure, the observed inverse genetic association with mucinous ovarian cancer is inferred to mean that alcohol intake may be a risk factor for this histotype. 29247577

2018