XRCC1, X-ray repair cross complementing 1, 7515

N. diseases: 410; N. variants: 39
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0001430
Disease: Adenoma
Adenoma
0.030 GeneticVariation group BEFREE The XRCC1 399Gln allele was associated with a reduction of risk of high-risk adenomas (OR 0.62, 95% CI 0.41-0.96). 16542436 2006
CUI: C0001430
Disease: Adenoma
Adenoma
0.030 GeneticVariation group BEFREE We have previously reported an inverse association between the XRCC1 codon 399 SNP and adenoma risk among these subjects. 17164360 2006
CUI: C1302401
Disease: Adenoma of large intestine
Adenoma of large intestine
0.030 GeneticVariation disease BEFREE Using a large sigmoidoscopy-based case-control study (753 cases and 799 controls) in Los Angeles County, we investigated possible associations between single-nucleotide polymorphisms in the XRCC1 (codons 194 Arg/Trp and codon 399 Arg/Gln) and XRCC3 (codon 241 Thr/Met) genes and colorectal adenoma risk and their possible role as modifiers of the effect of monounsaturated fatty acid, the ratio of omega-6/omega-3 polyunsaturated fatty acids, and antioxidant intake. 15767338 2005
CUI: C1302401
Disease: Adenoma of large intestine
Adenoma of large intestine
0.030 GeneticVariation disease BEFREE This study suggests that polymorphisms in APEX1, XRCC1, and PARP1 may be associated with advanced colorectal adenoma. 17283177 2007
CUI: C1302401
Disease: Adenoma of large intestine
Adenoma of large intestine
0.030 GeneticVariation disease BEFREE Polymorphisms of the XRCC1, XRCC3 and XPD genes and risk of colorectal adenoma and carcinoma, in a Norwegian cohort: a case control study. 16542436 2006
CUI: C0206623
Disease: Adenosquamous carcinoma
Adenosquamous carcinoma
0.010 GeneticVariation disease BEFREE In stratification analysis, significant elevated risk of adenocarcinoma/adenosquamous carcinoma was associated with the XRCC1 399GlnGln genotype among nonsmokers (OR = 3.85, 95% CI = 1.28-11.59, P = 0.017), but not among smokers. 15990162 2005
CUI: C1332201
Disease: Adult Diffuse Large B-Cell Lymphoma
Adult Diffuse Large B-Cell Lymphoma
0.020 GeneticVariation disease BEFREE In addition, the XRCC1 Arg194Trp polymorphism was associated with decreased NHL risk (Arg/Trp vs. Arg/Arg, OR: 0.72; 95% CI: 0.49-1.07; Trp/Trp vs. Arg/Arg, OR: 0.45; 95% CI: 0.10-1.99; p trend: 0.059), mainly in diffuse large B-cell lymphoma. 17666372 2007
CUI: C1332201
Disease: Adult Diffuse Large B-Cell Lymphoma
Adult Diffuse Large B-Cell Lymphoma
0.020 GeneticVariation disease BEFREE DNA repair gene XRCC1 polymorphisms and haplotypes in diffuse large B-cell lymphoma in a Korean population. 19963133 2010
CUI: C0278878
Disease: Adult Glioblastoma
Adult Glioblastoma
0.020 GeneticVariation disease BEFREE The highest odds ratios (ORs) for the associations were observed between the homozygous variant genotype XRCC1 Gln399Gln and the risk of glioma (OR = 1.32; 95% confidence interval, CI, 0.97-1.81), glioblastoma (OR = 1.48; 95% CI, 0.98-2.24), and meningioma (OR = 1.34; 95% CI, 0.96-1.86). 18330515 2008
CUI: C0278878
Disease: Adult Glioblastoma
Adult Glioblastoma
0.020 GeneticVariation disease BEFREE In the present study, we evaluated the association between polymorphisms in DNA repair genes, namely: XRCC1 rs25487, XRCC3 rs861539 and RAD51 rs1801320, with the susceptibility to develop glioblastoma. 26511493 2016
CUI: C0279607
Disease: Adult Hepatocellular Carcinoma
Adult Hepatocellular Carcinoma
0.010 GeneticVariation disease BEFREE This meta-analysis suggests the participation of XRCC1 Arg399Gln is a genetic susceptibility for hepatocellular cancer in Asians and breast cancer in Indians. 24205095 2013
CUI: C0220597
Disease: Adult Hodgkin Lymphoma
Adult Hodgkin Lymphoma
0.010 GeneticVariation disease BEFREE We observed that, in combination, allelic variants in the XPC Ala499Val, NBN Glu185Gln, XRCC3 Thr241Me, XRCC1 Arg194Trp, and XRCC1 399Gln polymorphisms modify the risk for developing HL. 21374732 2011
CUI: C0220630
Disease: Adult Liver Carcinoma
Adult Liver Carcinoma
0.030 AlteredExpression disease BEFREE Surprisingly, we found that low ALDH2 expression levels associated with high XRCC1 expression levels are indicative for a poor overall survival, particularly in lung and liver cancer patients. 30088263 2018
CUI: C0220630
Disease: Adult Liver Carcinoma
Adult Liver Carcinoma
0.030 Biomarker disease BEFREE We aimed to establish whether XRCC1, XRCC3, and XPD are associated with liver cancer in Pakistan and to examine the interaction of hepatitis B virus (HBV) or hepatitis C virus (HCV) with repaired genes in the occurrence of liver cancer. 23044807 2013
CUI: C0220630
Disease: Adult Liver Carcinoma
Adult Liver Carcinoma
0.030 GeneticVariation disease BEFREE Trial sequential analysis (TSA), false-positive report probabilities (FPRP), and combined genotype analysis revealed that XRCC1 Arg399Gln is mainly associated with susceptibility to liver cancer. 30408066 2018
CUI: C1332206
Disease: Adult Lymphoma
Adult Lymphoma
0.030 GeneticVariation disease BEFREE DNA repair gene XPD and XRCC1 polymorphisms and the risk of febrile neutropenia and mucositis in children with leukemia and lymphoma. 22047709 2012
CUI: C1332206
Disease: Adult Lymphoma
Adult Lymphoma
0.030 GeneticVariation disease BEFREE In this work, we retrospectively evaluated the influence of an XRCC1 polymorphism (rs25487) on the treatment results in a series of 73 patients with lymphoma subjected to ASCT. 21463129 2011
CUI: C1332206
Disease: Adult Lymphoma
Adult Lymphoma
0.030 GeneticVariation disease BEFREE DNA repair gene XRCC1 polymorphisms could lead to defective DNA repair and increased risk of lymphoma. 19963133 2010
CUI: C0278877
Disease: Adult Meningioma
Adult Meningioma
0.020 GeneticVariation disease BEFREE Furthermore, the genotype of CAPS8, XRCC1, and NF2 was associated with different subtype of meningioma risk. 29581016 2018
CUI: C0278877
Disease: Adult Meningioma
Adult Meningioma
0.020 GeneticVariation disease BEFREE However, in pair-wise comparisons a few SNP combinations were associated with the risk of brain tumors: Among others, carriers of both homozygous variant genotypes, i.e., XRCC1 Gln399Gln and XRCC3 Met241Met, were associated with a three-fold increased risk of glioma (OR = 3.18; 95% CI, 1.26-8.04) and meningioma (OR = 2.99; 95% CI, 1.16-7.72). 18330515 2008
CUI: C3900098
Disease: Adult Myelodysplastic Syndrome
Adult Myelodysplastic Syndrome
0.010 GeneticVariation disease BEFREE Association of XPD (Lys751Gln) and XRCC1 (Arg280His) gene polymorphisms in myelodysplastic syndrome. 26482462 2016
CUI: C0220605
Disease: Adult Non-Hodgkin Lymphoma
Adult Non-Hodgkin Lymphoma
0.020 GeneticVariation disease BEFREE DNA repair gene XRCC1 polymorphisms and non-Hodgkin lymphoma risk in a Chinese population. 19446740 2009
CUI: C0220605
Disease: Adult Non-Hodgkin Lymphoma
Adult Non-Hodgkin Lymphoma
0.020 GeneticVariation disease BEFREE Genetic polymorphisms in the DNA repair gene, XRCC1 associate with non-Hodgkin lymphoma susceptibility: A systematic review and meta-analysis. 26723520 2016
CUI: C4524268
Disease: Advanced lung cancer
Advanced lung cancer
0.020 GeneticVariation disease BEFREE Predictive assessment in pharmacogenetics of XRCC1 gene on clinical outcomes of advanced lung cancer patients treated with platinum-based chemotherapy. 26585370 2015
CUI: C4524268
Disease: Advanced lung cancer
Advanced lung cancer
0.020 GeneticVariation disease BEFREE The predictability of DNA repair XRCC1 (X-ray repair cross-complementing group 1 protein) single nucleotide polymorphisms (SNPs) for cisplatin-based grades 3 and 4 chemotherapy-related toxicity in patients with newly diagnosed advanced lung cancer was evaluated. 18400332 2008