Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1052133
rs1052133
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms
0.030 GeneticVariation BEFREE This meta-analysis on hOGG1 Ser326Cys polymorphism and the risk of EC suggests there is no statistically significant association between the two. 31700874

2019

dbSNP: rs1052133
rs1052133
CUI: C0546837
Disease: Malignant neoplasm of esophagus
Malignant neoplasm of esophagus
0.030 GeneticVariation BEFREE This meta-analysis on hOGG1 Ser326Cys polymorphism and the risk of EC suggests there is no statistically significant association between the two. 31700874

2019

dbSNP: rs1052133
rs1052133
CUI: C0152018
Disease: Esophageal carcinoma
Esophageal carcinoma
0.030 GeneticVariation BEFREE This meta-analysis on hOGG1 Ser326Cys polymorphism and the risk of EC suggests there is no statistically significant association between the two. 31700874

2019

dbSNP: rs1052133
rs1052133
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung
0.100 GeneticVariation BEFREE Using the multifactor dimensionality reduction method, we found a model of gene-gene interactions associated with the risk of lung cancer: NBS1 (rs1805794)-XRCC1 (rs25487)-hOGG1 (rs1052133)-XPG (rs17655). 31584889

2019

dbSNP: rs1052133
rs1052133
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung
0.100 GeneticVariation BEFREE Using the multifactor dimensionality reduction method, we found a model of gene-gene interactions associated with the risk of lung cancer: NBS1 (rs1805794)-XRCC1 (rs25487)-hOGG1 (rs1052133)-XPG (rs17655). 31584889

2019

dbSNP: rs1052133
rs1052133
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung
0.100 GeneticVariation BEFREE Using the multifactor dimensionality reduction method, we found a model of gene-gene interactions associated with the risk of lung cancer: NBS1 (rs1805794)-XRCC1 (rs25487)-hOGG1 (rs1052133)-XPG (rs17655). 31584889

2019

dbSNP: rs1052133
rs1052133
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung
0.100 GeneticVariation BEFREE To analyze the relationship of GSTT1, GSTM1, XRCC1 (rs25487), ERCC1 (rs11615, rs3212986), ERCC2 (rs13181), XRCC3 (rs861539), OGG1 (rs1052133), and Alpha-1-Antitrypsin mutations (AAT) with the risk of lung cancer in never-smokers, and ascertain if there is an effect modification between these polymorphisms and residential radon exposure. 31446980

2019

dbSNP: rs1052133
rs1052133
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung
0.100 GeneticVariation BEFREE To analyze the relationship of GSTT1, GSTM1, XRCC1 (rs25487), ERCC1 (rs11615, rs3212986), ERCC2 (rs13181), XRCC3 (rs861539), OGG1 (rs1052133), and Alpha-1-Antitrypsin mutations (AAT) with the risk of lung cancer in never-smokers, and ascertain if there is an effect modification between these polymorphisms and residential radon exposure. 31446980

2019

dbSNP: rs1052133
rs1052133
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung
0.100 GeneticVariation BEFREE To analyze the relationship of GSTT1, GSTM1, XRCC1 (rs25487), ERCC1 (rs11615, rs3212986), ERCC2 (rs13181), XRCC3 (rs861539), OGG1 (rs1052133), and Alpha-1-Antitrypsin mutations (AAT) with the risk of lung cancer in never-smokers, and ascertain if there is an effect modification between these polymorphisms and residential radon exposure. 31446980

2019

dbSNP: rs1052133
rs1052133
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
Non-Small Cell Lung Carcinoma
0.050 GeneticVariation BEFREE Taqman probe method was used to detect the genotypes of hOGG1 polymorphism locus rs1052133, with the genotype distribution frequencies of NSCLC group (P=0.411) and control group (P=0.354) consistent with the Hardy-Weinberg equilibrium. 31402936

2019

dbSNP: rs1052133
rs1052133
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.070 GeneticVariation BEFREE Urinary 8-hydroxydeoxyguanosine in relation to XRCC1 rs25487 G/A (Arg399Gln) and OGG1 rs1052133 C/G (Ser326Cys) DNA repair genes polymorphisms in patients with chronic hepatitis C and related hepatocellular carcinoma. 31354343

2019

dbSNP: rs1052133
rs1052133
CUI: C0524910
Disease: Hepatitis C, Chronic
Hepatitis C, Chronic
0.010 GeneticVariation BEFREE Urinary 8-hydroxydeoxyguanosine in relation to XRCC1 rs25487 G/A (Arg399Gln) and OGG1 rs1052133 C/G (Ser326Cys) DNA repair genes polymorphisms in patients with chronic hepatitis C and related hepatocellular carcinoma. 31354343

2019

dbSNP: rs1052133
rs1052133
CUI: C0019196
Disease: Hepatitis C
Hepatitis C
0.010 GeneticVariation BEFREE For OGG1 (Ser326Cys), GG (Cys/Cys) genotype and G-allele were increased significantly in chronic HCV and HCC patients compared to the controls (<i>P</i><0.05). 31354343

2019

dbSNP: rs1052133
rs1052133
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.060 GeneticVariation BEFREE It was concluded that oxidative DNA damage is increased in patients with Alzheimer's disease and OGG1 Ser326Cys polymorphism may be responsible for this increase. 31299287

2019

dbSNP: rs1052133
rs1052133
Childhood Acute Lymphoblastic Leukemia
0.030 GeneticVariation BEFREE The hOGG1 rs1052133 polymorphism is not associated with susceptibility to childhood ALL in the Taiwanese population. 31280195

2019

dbSNP: rs1052133
rs1052133
CUI: C0023473
Disease: Myeloid Leukemia, Chronic
Myeloid Leukemia, Chronic
0.010 GeneticVariation BEFREE OGG1 rs1052133 Polymorphism and Genetic Susceptibility to Chronic Myelogenous Leukaemia 30912416

2019

dbSNP: rs1052133
rs1052133
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.040 GeneticVariation BEFREE Our findings support associations of the hOGG1 Ser326Cys polymorphism with CSCC carcinogenesis and susceptibility to HR-HPV infection. 30648893

2019

dbSNP: rs1052133
rs1052133
CUI: C4048328
Disease: cervical cancer
cervical cancer
0.020 GeneticVariation BEFREE The hOGG1 Ser326Cys polymorphism may serve as a potential genetic biomarker of susceptibility to cervical cancer and HR-HPV infection. 30648893

2019

dbSNP: rs1052133
rs1052133
CUI: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix
0.020 GeneticVariation BEFREE The hOGG1 Ser326Cys polymorphism may serve as a potential genetic biomarker of susceptibility to cervical cancer and HR-HPV infection. 30648893

2019

dbSNP: rs1052133
rs1052133
CUI: C0302592
Disease: Cervix carcinoma
Cervix carcinoma
0.020 GeneticVariation BEFREE The hOGG1 Ser326Cys polymorphism may serve as a potential genetic biomarker of susceptibility to cervical cancer and HR-HPV infection. 30648893

2019

dbSNP: rs1052133
rs1052133
CUI: C0279671
Disease: Cervical Squamous Cell Carcinoma
Cervical Squamous Cell Carcinoma
0.010 GeneticVariation BEFREE Our findings support associations of the hOGG1 Ser326Cys polymorphism with CSCC carcinogenesis and susceptibility to HR-HPV infection. 30648893

2019

dbSNP: rs1052133
rs1052133
CUI: C0206708
Disease: Cervical Intraepithelial Neoplasia
Cervical Intraepithelial Neoplasia
0.010 GeneticVariation BEFREE hOGG1 Ser326Cys was genotyped through modified allele mismatch amplification polymerase chain reaction in 1200 healthy controls, 400 cervical intraepithelial neoplasia (CIN) grade III cases, and 400 CSCC cases. 30648893

2019

dbSNP: rs1052133
rs1052133
CUI: C0343641
Disease: Human papilloma virus infection
Human papilloma virus infection
0.010 GeneticVariation BEFREE Association of Base Excision Repair Gene hOGG1 Ser326Cys Polymorphism with Susceptibility to Cervical Squamous Cell Carcinoma and High-Risk Human Papilloma Virus Infection in a Chinese Population. 30648893

2019

dbSNP: rs1052133
rs1052133
CUI: C0030354
Disease: Papilloma
Papilloma
0.010 GeneticVariation BEFREE The hOGG1 Ser326Cys polymorphism may serve as a potential genetic biomarker of susceptibility to cervical cancer and HR-HPV infection. 30648893

2019

dbSNP: rs1052133
rs1052133
CUI: C0851140
Disease: Carcinoma in situ of uterine cervix
Carcinoma in situ of uterine cervix
0.010 GeneticVariation BEFREE We further observed enrichment of the hOGG1 Ser326Cys polymorphism in the CIN III (p = 0.021) and CSCC (p < 0.001) stratified by age at first intercourse, with more significant enrichment (p = 0.036) in the HR-HPV infection group. 30648893

2019