Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3218536
rs3218536
0.070 GeneticVariation BEFREE The XRCC2 R188H polymorphism was associated with a modest reduction in EOC risk: OR for heterozygotes was 0.8 (95% confidence interval [CI] = 0.7-1.0) and for rare homozygotes 0.3 (0.1-0.9). 15924337

2005

dbSNP: rs3218536
rs3218536
0.070 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
0.070 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
0.070 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
0.070 GeneticVariation BEFREE Interestingly, XRCC2 G>A (rs3218536) polymorphism might reduce the risk of ovarian cancer. 24599673

2014

dbSNP: rs3218536
rs3218536
0.070 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
0.070 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: 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

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: 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: rs2228001
rs2228001
XPC
0.010 GeneticVariation BEFREE Our results indicated that the XPC Lys939Gln polymorphism may correlate with clinical outcome of patients with epithelial ovarian cancer when treated with platinum-based chemotherapy in Northern China. 23621265

2013

dbSNP: rs56318008
rs56318008
0.010 GeneticVariation BEFREE The SNP rs56318008</span> was found to be strongly associated with EOC risk. 30457351

2018

dbSNP: rs1222213359
rs1222213359
0.020 GeneticVariation BEFREE The study suggested a possible association between the VEGF -1154G/A polymorphism with susceptibility to EOC, but there is no support for an association of the VEGF -460C/T, +936C/T, and -2578C/A polymorphisms with the risk for EOC. 20973260

2010

dbSNP: rs1222213359
rs1222213359
0.020 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 rs2228570 polymorphism increased the risk of ovarian cancer in Caucasian populations in a dominant genetic model. 29239065

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 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 The VDR polymorphism FokI (rs2228570) seems to increase the risk of ovarian cancer. 29113037

2017

dbSNP: rs1544410
rs1544410
VDR
0.020 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: rs1544410
rs1544410
VDR
0.020 GeneticVariation BEFREE The association of ovarian cancer risk with polymorphisms in the vitamin D receptor (VDR) gene, including rs10735810 (FokI), rs11568820 (Cdx-2), rs1544410 (BsmI), rs7975232 (ApaI), rs731236 (TaqI), and BsmI-ApaI-TaqI combined genotypes, was examined among 313 women with epithelial ovarian carcinoma and 574 controls. 18086759

2007