Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3218536
rs3218536
0.060 GeneticVariation BEFREE Overall, a significant association was found between the Arg188His polymorphism and ovarian cancer risk when all studies were pooled into the meta-analysis (Arg/Arg vs His/His: OR = 1.85, 95%CI = 1.15-3.00; Arg/Arg vs Arg/His: OR = 1.17, 95%CI = 1.03-1.32; dominant model: OR = 0.84, 95%CI = 0.74-0.95; recessive model: OR = 1.69, 95%CI = 1.05-2.70). 26400309

2015

dbSNP: rs3218536
rs3218536
0.060 GeneticVariation BEFREE In conclusion, this meta-analysis indicates that XRCC2 rs3218536 and ERCC2 rs13181 polymorphisms may not be associated with the risk of OC. 27863412

2016

dbSNP: rs3218536
rs3218536
0.060 GeneticVariation BEFREE The current meta-analysis indicated that the Arg188His polymorphism in the XRCC2 gene might be a risk factor for ovarian cancer. 24414483

2014

dbSNP: rs3218536
rs3218536
0.060 GeneticVariation BEFREE The aim of the present study was to evaluate the role of SNPs in three genes, XRCC2 (R188H), ERCC2 (K751Q) and CDKN1B (V109G) which are with moderate risk for ovarian cancer susceptibility in Egyptian women. 23277402

2013

dbSNP: rs3218536
rs3218536
0.060 GeneticVariation BEFREE The obtained results indicate that XRCC2 Arg188His and XRCC3 Thr241Met polymorphisms may be positively associated with the incidence of ovarian carcinoma in the population of Polish women. 26801223

2016

dbSNP: rs3218536
rs3218536
0.060 GeneticVariation BEFREE Interestingly, XRCC2 G>A (rs3218536) polymorphism might reduce the risk of ovarian cancer. 24599673

2014

dbSNP: rs587780128
rs587780128
0.010 GeneticVariation BEFREE These mutations and variants were detected in families with both breast and ovarian cancers, except for the RAD51B c.475C > T/p.Arg159Cys variant that occurred in a family with 3 breast cancer cases. 24139550

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

dbSNP: rs25487
rs25487
0.030 GeneticVariation BEFREE This study indicated that XRCC1 Arg194Trp, Arg280His, and Arg399Gln did not affect OS after platinum-based chemotherapy in OC patients. 30407287

2018

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: rs1799782
rs1799782
0.020 GeneticVariation BEFREE In conclusion, hOGG1 Ser326Cys and XRCC1 Arg194Trp polymorphisms may be regarded as risk factors of ovarian cancer. 26124010

2015

dbSNP: rs1799782
rs1799782
0.020 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: rs1222213359
rs1222213359
0.010 GeneticVariation BEFREE None of the five genetic models suggested a significant association between -1154G/A and ovarian cancer risk in the entire study population, or between +936C/T and risk in Asian or Chinese participants. 29069849

2017

dbSNP: rs2146323
rs2146323
0.010 GeneticVariation BEFREE VEGF tagSNPs rs3025033 and rs2146323 were not associated with ovarian cancer survival in the Australian sample. 20832104

2010

dbSNP: rs3025033
rs3025033
0.010 GeneticVariation BEFREE VEGF tagSNPs rs3025033 and rs2146323 were not associated with ovarian cancer survival in the Australian sample. 20832104

2010

dbSNP: rs2228570
rs2228570
VDR
0.050 GeneticVariation BEFREE The VDR polymorphism FokI (rs2228570) seems to increase the risk of ovarian cancer. 29113037

2017

dbSNP: rs2228570
rs2228570
VDR
0.050 GeneticVariation BEFREE This pooled analysis provides further evidence that the VDR rs2228570 polymorphism might influence ovarian cancer susceptibility. 20473893

2011

dbSNP: rs2228570
rs2228570
VDR
0.050 GeneticVariation BEFREE The homozygote model with the rs2228570 (FokI) polymorphism model appeared to detect the risk of OC in all cases, whereas the heterozygote model with the rs1544410 (BsmI) polymorphism seemed to detect the risk of OC in Caucasian patients. 30059751

2018

dbSNP: rs2228570
rs2228570
VDR
0.050 GeneticVariation BEFREE More studies are warranted to assess the association between the VDR rs2228570 polymorphism and ovarian cancer in Asians and Africans. 24136742

2014

dbSNP: rs2228570
rs2228570
VDR
0.050 GeneticVariation BEFREE The rs2228570 polymorphism increased the risk of ovarian cancer in Caucasian populations in a dominant genetic model. 29239065

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: 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: 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: rs4648551
rs4648551
0.010 GeneticVariation BEFREE We genotyped the p63 (rs873330 [Genbank, refSNP ID] T > C [T: original base, C: mutant base]) and p73 (rs4648551 G > A and rs6695978 G > A) SNPs in ovarian cancers and healthy controls and analyzed the distributions of genotype frequencies to evaluate the association of the genotypes with the risk of ovarian cancer and the clinicopathological characteristics. 23095717

2012

dbSNP: rs6695978
rs6695978
0.010 GeneticVariation BEFREE The p73 rs6695978 G > A polymorphism will serve as a modifier of ovarian cancer susceptibility and prognosis. 23095717

2012