Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs25487
rs25487
0.100 GeneticVariation BEFREE Haplotype analysis of XRCC1 Arg194Trp (C/T) and Arg399Gln (G/A) revealed that the frequency of the T-A haplotype was significantly higher in PC patients. 17196815

2007

dbSNP: rs25487
rs25487
0.100 GeneticVariation BEFREE Based on these results, the XRCC1-Arg399Gln polymorphism might be a risk factor for PCa and it could be considered as a prognostic and predictive biomarker for susceptible men. 30160806

2018

dbSNP: rs25487
rs25487
0.100 GeneticVariation BEFREE In summary, we suggest that XRCC1 Arg399Gln might be significantly associated with development of Pca. 25262700

2015

dbSNP: rs25487
rs25487
0.100 GeneticVariation BEFREE Among the three polymorphisms, we found that the XRCC1 Arg399Gln variant allele was associated with increased PCa risk (adjusted odd ratio [OR]: 1.67, 95% confident interval [CI]: 1.11-2.51), but the XRCC1 Arg194Trp variant allele had a 38% reduction in risk of PCa (adjusted OR: 0.62, 95% CI: 0.41-0.93). 17486273

2007

dbSNP: rs25487
rs25487
0.100 GeneticVariation BEFREE Overall, the results of this meta-analysis show that the XRCC1-Arg399Gln polymorphism may be associated with an increased risk for prostate cancer under the homozygote model and the recessive model. 25927275

2015

dbSNP: rs1799782
rs1799782
0.040 GeneticVariation BEFREE Overall, there was no obvious association between XRCC1 Arg194Trp polymorphism and prostate cancer</span> risk (Trp vs. Arg: OR = 1.02, 95%CI 0.84-1.25, P = 0.824; TrpTrp vs. ArgArg: OR = 1.17, 95%CI 0.83-1.66, P = 0.374; TrpTrp/ArgTrp vs. ArgArg: OR = 1.00, 95%CI 0.79-1.28, P = 0.990; TrpTrp vs. ArgArg/ArgTrp: OR = 1.20, 95%CI 0.85-1.68, P = 0.301). 24492938

2014

dbSNP: rs1799782
rs1799782
0.040 GeneticVariation BEFREE Among the three polymorphisms, we found that the XRCC1 Arg399Gln variant allele was associated with increased PCa risk (adjusted odd ratio [OR]: 1.67, 95% confident interval [CI]: 1.11-2.51), but the XRCC1 Arg194Trp variant allele had a 38% reduction in risk of PCa (adjusted OR: 0.62, 95% CI: 0.41-0.93). 17486273

2007

dbSNP: rs1799782
rs1799782
0.040 GeneticVariation BEFREE Haplotype analysis of XRCC1 Arg194Trp (C/T) and Arg399Gln (G/A) revealed that the frequency of the T-A haplotype was significantly higher in PC patients. 17196815

2007

dbSNP: rs1799782
rs1799782
0.040 GeneticVariation BEFREE In this meta-analysis, we found that both Arg399Gln and Arg194Trp polymorphisms were not related to overall PCa risk. 21647176

2011

dbSNP: rs25489
rs25489
0.030 GeneticVariation BEFREE However, there was no significant risk of PCa associated with Arg280His polymorphism. 17486273

2007

dbSNP: rs25489
rs25489
0.030 GeneticVariation BEFREE And XRCC1-Arg280His polymorphism is likely to be related with prostate cancer risk under the heterozygote model and the dominant model. 25927275

2015

dbSNP: rs25489
rs25489
0.030 GeneticVariation BEFREE We conclude that the XRCC1 Arg280His polymorphism may be protective against the development of high-grade late toxicity after radiotherapy in prostate cancer patients. 21345510

2011

dbSNP: rs1041258260
rs1041258260
0.010 GeneticVariation BEFREE The aim of the present study was to analyze the effect of XPG Asp 1104His and XRCC1 Arg309Gln polymorphisms on risk of prostate cancer in north Indian population. 21670956

2012

dbSNP: rs25490
rs25490
0.010 GeneticVariation BEFREE These findings suggest that the c.910A>G polymorphism of the XRCC1 gene is associated with susceptibility to Pca in Chinese men, the G-allele conferring higher risk. 23244143

2012

dbSNP: rs777272152
rs777272152
0.010 GeneticVariation BEFREE The aim of the present study was to analyze the effect of XPG Asp 1104His and XRCC1 Arg309Gln polymorphisms on risk of prostate cancer in north Indian population. 21670956

2012

dbSNP: rs1870134
rs1870134
XPC ; LSM3
0.010 GeneticVariation BEFREE Among these eight SNPs investigated, only XPC rs1870134 CG/CC variant genotypes were associated with a decreased risk of prostate cancer under a dominant genetic model (adjusted odds ratio [OR] = 0.77, 95% confidence interval [CI] = 0.64-1.91, P = 0.003). 27974699

2017

dbSNP: rs2228001
rs2228001
XPC
0.050 GeneticVariation BEFREE The combined analysis of XPC Lys939Gln and XPC-PAT variants showed that patients who inherited (Lys/Gln + PAT D/D) genotypes were protected against prostate cancer development compared to controls. 30552616

2019

dbSNP: rs2228001
rs2228001
XPC
0.050 GeneticVariation BEFREE These analyses suggest that XPC gene PAT+/-polymorphism, but not rs2228001, likely contributes to susceptibility to PCa. 24093803

2013

dbSNP: rs2228001
rs2228001
XPC
0.050 GeneticVariation BEFREE This is the first report on the studies of XPC and XRCC1 Arg194Trp polymorphisms in PC, and our present data suggest that XPC Lys939Gln and the T-A haplotype of XRCC1 Arg194Trp and Arg399Gln may be risk factors for PC in Japanese. 17196815

2007

dbSNP: rs2228001
rs2228001
XPC
0.050 GeneticVariation BEFREE The purpose of this study was to evaluate the relationship between single-nucleo­tide polymorphism (SNP) rs2228001 in xeroderma pigmentosum group C (XPC), SNP rs4073 in interleukin 8 (IL8), and SNP rs2279744 in mouse double minute 2 (MDM2) homolog gene with PCa susceptibility. 26135929

2015

dbSNP: rs2228001
rs2228001
XPC
0.050 GeneticVariation BEFREE Analyses of the XPC Lys939Gln polymorphism did not show an association with PCa risk. 22682619

2012

dbSNP: rs2807031
rs2807031
C 0.700 GeneticVariation GWASCAT Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci. 29892016

2018

dbSNP: rs2807031
rs2807031
C 0.700 GeneticVariation GWASCAT A meta-analysis of 87,040 individuals identifies 23 new susceptibility loci for prostate cancer. 25217961

2014

dbSNP: rs114780236
rs114780236
G 0.700 GeneticVariation GWASCAT 12 new susceptibility loci for prostate cancer identified by genome-wide association study in Japanese population. 31562322

2019

dbSNP: rs619824
rs619824
0.010 GeneticVariation BEFREE Moreover, our study suggests that rs619824 and rs2486758 polymorphisms are associated with PCa risk. 21656827

2011