Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1042522
rs1042522
0.040 GeneticVariation BEFREE Meta-analysis shows significant association of the TP53 Arg72Pro with ovarian cancer risk. 21952824

2012

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

2014

dbSNP: rs144848
rs144848
0.040 GeneticVariation BEFREE There was no association between BRCA2 N372H and risk of borderline or invasive epithelial ovarian cancer. 14555511

2003

dbSNP: rs144848
rs144848
0.040 GeneticVariation BEFREE The HH genotype of the nonconservative amino acid substitution polymorphism N37</span>2H in the BRCA2 gene was reported to be associated with a 1.3- to 1.5-fold increase in risk of both breast and ovarian cancer. 15668505

2005

dbSNP: rs144848
rs144848
0.040 GeneticVariation BEFREE Moreover, stratified analyses by the cancer type and source of control observed significantly increased risk associated with BRCA2 N372H in subgroups with ovarian cancer, non-Hodgkin lymphoma and population-based controls, but not breast cancer or hospital-based controls. 25348552

2014

dbSNP: rs144848
rs144848
0.040 GeneticVariation BEFREE The subgroup analysis for serous cancer subgroup showed that the significant association could be detected under recessive model (OR = 1.38, 95% CI, 1.01-1.89, P = 0.04) and under homozygote comparison (OR = 1.46, 95% CI, 1.06-2.01, P = 0.022).Our meta-analysis suggests that the N372H polymorphism is associated with susceptibility of ovarian cancer. 26496279

2015

dbSNP: rs1799950
rs1799950
0.040 GeneticVariation BEFREE Further characterisation of rs1799950 is now warranted in relation to chemosensitivity and susceptibility to developing ovarian carcinoma. 29298688

2018

dbSNP: rs1799950
rs1799950
0.040 GeneticVariation BEFREE No association was detected between EOC risk and BRCA1 Q356R, BRCA1 P871L, RAD51 g135c, RAD51 g172t, RAD52 c2259t, NBS1 L34L, NBS1 E185Q, NBS1 A399A, NBS1 P672P, XRCC2 g4324c, XRCC2 c41657t and XRCC3 T241M. 15924337

2005

dbSNP: rs1799950
rs1799950
0.040 GeneticVariation BEFREE The rare form of the Q356R polymorphism was significantly ( P = 0.03) associated with a family history of ovarian cancer, suggesting that this polymorphism may influence ovarian cancer risk. 10196379

1999

dbSNP: rs1799950
rs1799950
0.040 GeneticVariation BEFREE We resequenced BRCA1 and BRCA2 in 194 women with a familial history of breast and/or ovarian cancer and identified nine possibly biologically relevant polymorphisms (BRCA1 Gln356Arg, Pro871Leu, Glu1038Gly, Ser1613Gly, and Met1652Ile. 19661094

2009

dbSNP: rs397507444
rs397507444
0.040 GeneticVariation BEFREE In conclusion, the results of this meta-analysis indicate that the MTHFR C677T and A1298C polymorphisms are not associated with ovarian cancer risk, especially in Caucasians. 22810649

2012

dbSNP: rs397507444
rs397507444
0.040 GeneticVariation BEFREE In conclusion, this meta-analysis suggests that the A1298C polymorphism in the MTHFR gene may be not associated with susceptibility to ovarian cancer. 26345746

2015

dbSNP: rs397507444
rs397507444
0.040 GeneticVariation BEFREE In addition, there is no association between A1298C gene polymorphism and ovarian cancer, including Caucasian and Asian women. 24720627

2014

dbSNP: rs397507444
rs397507444
0.040 GeneticVariation BEFREE Overall, we observed no association between either SNP and ovarian cancer risk (pooled C677T p(trend)=0.59 and A1298C p(</span>trend)=0.58). 20817226

2010

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: rs1271572
rs1271572
0.030 GeneticVariation BEFREE The recessive model of ESR2 rs1271572 and the dominant model of ESR2 rs3020450 might be susceptible factors for ovarian cancer. 29535531

2018

dbSNP: rs1271572
rs1271572
0.030 GeneticVariation BEFREE Compared to homozygous common allele carriers, homozygous carriers of variant alleles for rs1271572 [odds ratio (OR) = 1.79, 95% confidence interval (CI):1.15-2.79, p global = 0.01] and rs1256030 [OR = 1.67, CI: 1.08-2.59, p global = 0.04], and women with haplotypes, including variant alleles of rs1271572, rs1256030, and rs1256031 SNPs [OR = 1.75, CI: 1.17-2.63, p global = 0.007], had significantly increased risk of ovarian carcinoma. 18704709

2009

dbSNP: rs1271572
rs1271572
0.030 GeneticVariation BEFREE This pooled analysis suggests that rs1271572 might influence the risk of ovarian cancer, in particular among younger women. 21673961

2011

dbSNP: rs2032582
rs2032582
0.030 GeneticVariation BEFREE The mdr-1 polymorphism G2677T/A in exon 21 correlates with the paclitaxel response in ovarian cancer and may be important for the function of P-glycoprotein and resistance to paclitaxel and provide useful information for individualized therapy. 16467099

2006

dbSNP: rs2032582
rs2032582
0.030 GeneticVariation BEFREE Genetic polymorphisms such as ERCC1 8092C>A, ABCB1 2677G>T/A, GSTP1 I105V and GSTT1 polymorphisms may affect drug response, toxicity and survival in patient with EOC who received taxane- and platinum-based chemotherapy after surgery. 19203783

2009

dbSNP: rs2032582
rs2032582
0.030 GeneticVariation BEFREE Our study represents the largest analysis of ABCB1 SNPs and EOC progression and survival to date, but has not identified additional signals, or validated reported associations with progression-free survival for rs1128503, rs2032582, and rs1045642. 23917080

2013

dbSNP: rs25487
rs25487
0.030 GeneticVariation BEFREE Our study found a significant association between XRCC1 Arg399Gln and XRCC1 Arg194Trp polymorphism and the clinical outcome of ovarian cancer. 22983827

2013

dbSNP: rs25487
rs25487
0.030 GeneticVariation BEFREE Impact of RAD51 G135C and XRCC1 Arg399Gln polymorphisms on ovarian carcinoma risk in Serbian women. 26406958

2015