Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
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: 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: 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: 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: 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

dbSNP: rs1052133
rs1052133
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
0.010 GeneticVariation BEFREE Our aim was to evaluate the association of the OGG1-rs1052133 with total, cancer, and cardiovascular disease (CVD) mortality and to analyze its modulation by the Mediterranean diet, focusing especially on total vegetable intake as one of the main characteristics of this diet. 29305130

2018

dbSNP: rs1052133
rs1052133
CUI: C0345967
Disease: Malignant mesothelioma
Malignant mesothelioma
0.010 GeneticVariation BEFREE Although there was no independent association between either <i>CAT</i> rs1001179 or <i>hOGG1</i> rs1052133 polymorphism and malignant mesothelioma, interaction between both polymorphisms showed a protective effect, OR<sub>int</sub> 0.27 (95% CI 0.10-0.77). 29520212

2018

dbSNP: rs1052133
rs1052133
CUI: C0027708
Disease: Nephroblastoma
Nephroblastoma
0.010 GeneticVariation BEFREE Significant associations with Wilms tumor susceptibility were shown for hOGG1 rs1052133 (dominant: adjusted OR = 0.66, 95% CI = 0.45-0.96, P = .030), FEN1 rs174538 (dominant: adjusted OR = 0.66, 95% CI = 0.45-0.95, P = .027; recessive: adjusted OR = 0.54, 95% CI = 0.32-0.93 P = .027), and FEN1 rs4246215 (dominant: adjusted OR = 0.55, 95% CI = 0.38-0.80, P = .002) polymorphisms. 29937070

2018

dbSNP: rs1052133
rs1052133
CUI: C1333015
Disease: Childhood Kidney Wilms Tumor
Childhood Kidney Wilms Tumor
0.010 GeneticVariation BEFREE Significant associations with Wilms tumor susceptibility were shown for hOGG1 rs1052133 (dominant: adjusted OR = 0.66, 95% CI = 0.45-0.96, P = .030), FEN1 rs174538 (dominant: adjusted OR = 0.66, 95% CI = 0.45-0.95, P = .027; recessive: adjusted OR = 0.54, 95% CI = 0.32-0.93 P = .027), and FEN1 rs4246215 (dominant: adjusted OR = 0.55, 95% CI = 0.38-0.80, P = .002) polymorphisms. 29937070

2018

dbSNP: rs1052133
rs1052133
CUI: C0027819
Disease: Neuroblastoma
Neuroblastoma
0.010 GeneticVariation BEFREE Stratified analysis revealed that rs1052133</span> GC/CC carriers were less likely to develop neuroblastoma in subgroups of age >18 months, males, tumor that develops from retroperitoneal, mediastinum and clinical stage I+II+4s. 30519358

2018

dbSNP: rs1052133
rs1052133
CUI: C0848676
Disease: Subfertility, Male
Subfertility, Male
0.010 GeneticVariation BEFREE The hOGG1 Ser326Cys polymorphism and male subfertility in Taiwanese patients with varicocele. 29582449

2018

dbSNP: rs1052133
rs1052133
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.010 GeneticVariation BEFREE The OGG1 S326C CC genotype (associated with lower OGG1 activity) was observed more frequently in patients with AML relapse [28.9 vs. 8.9%, odds ratio (OR) = 4.10, 95% confidence interval (CI) = 1.35-12.70, P = 0.01]. 29737460

2018

dbSNP: rs1052133
rs1052133
CUI: C0280324
Disease: Laryngeal Squamous Cell Carcinoma
Laryngeal Squamous Cell Carcinoma
0.010 GeneticVariation BEFREE Our meta-analysis results indicated that <i>hOGG1</i> Ser326Cys polymorphism may be associated with increased risk of HNSCC, especially in Caucasians, alcohol drinkers and the patients with laryngeal squamous cell carcinoma. 29560133

2018

dbSNP: rs1052133
rs1052133
CUI: C0042341
Disease: Varicocele
Varicocele
0.010 GeneticVariation BEFREE The hOGG1 Ser326Cys polymorphism and male subfertility in Taiwanese patients with varicocele. 29582449

2018

dbSNP: rs1052133
rs1052133
CUI: C4086165
Disease: Childhood Neuroblastoma
Childhood Neuroblastoma
0.010 GeneticVariation BEFREE Stratified analysis revealed that rs1052133</span> GC/CC carriers were less likely to develop neuroblastoma in subgroups of age >18 months, males, tumor that develops from retroperitoneal, mediastinum and clinical stage I+II+4s. 30519358

2018

dbSNP: rs1052133
rs1052133
CUI: C0028754
Disease: Obesity
Obesity
0.010 GeneticVariation BEFREE This study investigated the associations of OGG1 Ser326Cys SNP in relation to HIV and obes</span>ity on the susceptibility of low-birthweight (LBW) and pre-term birth (PTB) in SA women exposed to ambient air-pollution living in Durban. 29709520

2018

dbSNP: rs1052133
rs1052133
CUI: C0700095
Disease: Central neuroblastoma
Central neuroblastoma
0.010 GeneticVariation BEFREE Stratified analysis revealed that rs1052133</span> GC/CC carriers were less likely to develop neuroblastoma in subgroups of age >18 months, males, tumor that develops from retroperitoneal, mediastinum and clinical stage I+II+4s. 30519358

2018

dbSNP: rs1052133
rs1052133
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma
0.010 GeneticVariation BEFREE No significant association was observed between hOGG1 Ser326Cys and ITGA2 C807T polymorphisms with NPC risk after adjustment for age, gender, ethnicity, cigarette smoking, alcohol and salted fish consumption. 29121049

2017

dbSNP: rs1052133
rs1052133
CUI: C0007113
Disease: Rectal Carcinoma
Rectal Carcinoma
0.010 GeneticVariation BEFREE Subgroup analyses revealed significant association of OGG1 rs1052133 with rectal cancer risk. 28749454

2017

dbSNP: rs1052133
rs1052133
CUI: C0595921
Disease: Intraocular pressure disorder
Intraocular pressure disorder
0.010 GeneticVariation BEFREE Furthermore, there were thicker corneas, higher intraocular pressure (IOP) and a shorter axial length in patients carrying the mutant genotypes of <i>hOGG1</i> Ser326Cys (Ser/Cys + Cys/Cys), <i>APE1</i> Asp148Glu (Asp/Glu + Glu/Glu) and XRCC<i>1</i> Arg399Gln (Arg/Gln + Glu/Glu) than those carrying the corresponding wild-type genotypes. 28396513

2017

dbSNP: rs1052133
rs1052133
Squamous cell carcinoma of oropharynx
0.010 GeneticVariation BEFREE We examined the influence of OGG1 c.977C>G (rs1052133), APEX1 c.444T>G (rs1130409), XRCC1 c.-77T>C (rs3213245), c.580C>T (rs1799782), c.839G>A (rs25489) and c.1196G>A (rs25487) single-nucleotide polymorphisms (SNPs), involved in base-excision repair (BER) pathway, on oropharyngeal squamous cell carcinoma (OPSCC) risk and prognosis. 27372710

2016

dbSNP: rs1052133
rs1052133
CUI: C0751075
Disease: Cancer of Digestive System
Cancer of Digestive System
0.010 GeneticVariation BEFREE In our analysis, the hOGG1 Ser326Cys polymorphism was significantly associated with the risk of digestive system cancers (Cys/Cys vs. Ser/Ser: OR = 1.17, 95% CI = 1.00-1.35, P < 0.001; Cys/Cys vs. Cys/Ser + Ser/Ser: OR = 1.14, 95% CI = 1.00-1.29, P < 0.001). 25323581

2015