Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.400 GeneticVariation disease BEFREE These results suggest that the CYP1A2 -3860G>A polymorphism modifies the smoking-related HCC risk among CLD patients. 19643819 2009
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.400 GeneticVariation disease BEFREE No significant association between CYP1A2 genetic polymorphisms and HCC risk was observed in either HBsAg seropositive individuals or non-smokers. 16495781 2006
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.400 GeneticVariation disease BEFREE Since Qidong is a special region with particularly high incidence of hepatocellular carcinoma in China, the association of phenotypes with genotypes of CYP1A2 in the Qidong population might result from some inducible environmental factors such as those of cigarettes in smokers. 11470995 2001
CUI: C0162566
Disease: Porphyria Cutanea Tarda
Porphyria Cutanea Tarda
0.360 GeneticVariation disease BEFREE The CYP1A2*1F promoter A allele frequency was significantly higher (P < 0.022) and the A/A genotype frequency marginally higher in PCT patients overall (P < 0.057), with the A/A genotype significantly more common in type 1 PCT (P < 0.043). 20957336 2011
CUI: C0162566
Disease: Porphyria Cutanea Tarda
Porphyria Cutanea Tarda
0.360 GeneticVariation disease BEFREE We found an increase in the frequency of CYP1A2 g-163A allele in patients with PCT when compared with controls, although the more inducible A/A genotype had no effect on the onset age. 20163457 2010
CUI: C0162566
Disease: Porphyria Cutanea Tarda
Porphyria Cutanea Tarda
0.360 GeneticVariation disease BEFREE Association of CYP1A2 polymorphisms with susceptibility to both types of PCT has already been described in Danish patients. 14714565 2003
CUI: C0162566
Disease: Porphyria Cutanea Tarda
Porphyria Cutanea Tarda
0.360 GeneticVariation disease BEFREE In this study, we have examined a group of Danish patients with PCT for the presence of the C/A polymorphism in intron 1 of CYP1A2. 11153915 2000
CUI: C0007137
Disease: Squamous cell carcinoma
Squamous cell carcinoma
0.330 GeneticVariation disease BEFREE There was however no significant increased risk of developing lung SCC in smokers having CYP1A2 gene polymorphisms. 19332078 2009
CUI: C0007137
Disease: Squamous cell carcinoma
Squamous cell carcinoma
0.330 GeneticVariation disease BEFREE Our data also revealed that smokers or tobacco chewers carrying variant alleles of either CYP1A2*1D or CYP1A2*1F were at increased risk to SCC of lung, further demonstrating that CYP1A2 genotypes interact with environmental risk factors in enhancing the risk to squamous cell lung carcinoma. 22072123 2012
CUI: C0007137
Disease: Squamous cell carcinoma
Squamous cell carcinoma
0.330 GeneticVariation disease BEFREE A significant interaction between CYP1A2-T/delT or delT/delT genotypes and tobacco consumption (pack-years) adjusted for age was evident (OR (95% CI) 7.78 (1.52-42.8)) in the SCC cases who smoked relatively less (< or =33 pack-years, I quartile value), but not in adenocarcinoma and controls. 17509724 2007
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease
0.330 GeneticVariation disease BEFREE CYP1A1, CYP1A2 and CYBA gene polymorphisms associated with oxidative stress in COPD. 20080081 2010
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease
0.330 GeneticVariation disease BEFREE In conclusion, our data suggest that genetic alterations in CYP1A2 may play a role both in the pharmacogenetics of TP and in the development of COPD. 20797314 2010
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease
0.330 GeneticVariation disease LHGDN The (-2467)delT allele and CYP1A2*1D haplotype of CYPIA2 gene was associated with higher risk of COPD in Tatar ethnic group (OR = 1.83, 95% CI 1.24-2.71, chi2 = 9.48, p = 0.003 and chi2 = 9.733, p = 0.0027, Pcor = 0.008; OR = 3.908, 95% CI 1.56-10.19, respectively). 18389617 2008
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms
0.320 GeneticVariation group LHGDN Polymorphisms in the cytochrome P450 genes CYP1A2, CYP1B1, CYP3A4, CYP3A5, CYP11A1, CYP17A1, CYP19A1 and colorectal cancer risk. 17615053 2007
CUI: C0024121
Disease: Lung Neoplasms
Lung Neoplasms
0.320 GeneticVariation group LHGDN NAT2 and CYP1A2 polymorphisms and lung cancer risk in relation to smoking status. 17477782 2007
CUI: C0809983
Disease: Schizophrenia and related disorders
Schizophrenia and related disorders
0.310 GeneticVariation group BEFREE In this study we explored possible epistasis between CYP2D6 (*3, *4, *5, *6 and *1xN), CYP3A5 (*3), CYP1A2 (*1C and *1F) and ABCB1 (G2677T) in schizophrenia and related disorders. 21142916 2010
CUI: C0860207
Disease: Drug-Induced Liver Disease
Drug-Induced Liver Disease
0.310 GeneticVariation phenotype BEFREE The frequency of the CYP1A2 1F allele was 63.9% in P. multiflorum-induced DILI patients, compared to 57.0% in healthy controls; the difference was not significant. 25117321 2014
CUI: C0005695
Disease: Bladder Neoplasm
Bladder Neoplasm
0.100 GeneticVariation disease BEFREE To test the hypothesis that variation in the genes that metabolize tobacco carcinogens contribute to bladder cancer, we examined the effects of single nucleotide polymorphisms in the genes of four key enzymes: cytochrome P450 1A2, N-acetyltransferase (NAT) 2, sulfotransferase 1A1, and UDP-glucuronosyltransferase (UGT) 2B7. 22961351 2013
CUI: C0005695
Disease: Bladder Neoplasm
Bladder Neoplasm
0.100 GeneticVariation disease BEFREE We conclude that the CYP1A2-163C/A polymorphism is associated with increased susceptibility to bladder cancer in the Chinese population. 27173252 2016
CUI: C0005695
Disease: Bladder Neoplasm
Bladder Neoplasm
0.100 GeneticVariation disease LHGDN Genetic polymorphisms of cytochrome P450 CYP1A1 (*2A) and microsomal epoxide hydrolase gene, interactions with tobacco-users, and susceptibility to bladder cancer: a study from North India. 18200441 2008
CUI: C0005695
Disease: Bladder Neoplasm
Bladder Neoplasm
0.100 GeneticVariation disease BEFREE Subjects possessing the NAT2 slow acetylation phenotype and the highest tertile of CYP1A2 scores showed the highest risk for bladder cancer. 21480221 2012
CUI: C0005695
Disease: Bladder Neoplasm
Bladder Neoplasm
0.100 GeneticVariation disease BEFREE Within the framework of a hospital-based case/control study, we investigated the relationship between CYP1A2 polymorphisms, occupational/environmental exposures and bladder cancer (BC) risk. 20559687 2010
CUI: C0005695
Disease: Bladder Neoplasm
Bladder Neoplasm
0.100 GeneticVariation disease BEFREE In summary, this meta-analysis suggests that CYP1A2*1F polymorphism is associated with lung cancer and bladder cancer risk in Caucasians. 25472037 2015
CUI: C0005695
Disease: Bladder Neoplasm
Bladder Neoplasm
0.100 GeneticVariation disease BEFREE Recently, a C/A-polymorphism in intron 1 of cytochrome P450 1A2 was associated with high inducibility and persons with this high inducibility variant were overrepresented in bladder cancer, but only if they were smokers or if they had slow NAT2 genotypes. 10022251 1998
CUI: C0005695
Disease: Bladder Neoplasm
Bladder Neoplasm
0.100 GeneticVariation disease BEFREE The results from the meta-analysis suggested that the CYP1A2 rs762551 polymorphism is a protective factor for bladder cancer, especially in Caucasians. 26514519 2015