Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1278748858
rs1278748858
Entrez Id: 1544
Gene Symbol: CYP1A2
CYP1A2
CUI: C0006142
Disease:
Malignant neoplasm of breast
0.010 GeneticVariation BEFREE The results of the study suggest that NQO1 exon 6 proline187serine (C609T) and CYP1A2 exon 2 phenylalanine21leucine (C63G) polymorphisms do not play a significant role in breast cancer susceptibility in North Indian women. 21329464 2011
dbSNP: rs1278748858
rs1278748858
Entrez Id: 1544
Gene Symbol: CYP1A2
CYP1A2
CUI: C0678222
Disease:
Breast Carcinoma
0.010 GeneticVariation BEFREE The results of the study suggest that NQO1 exon 6 proline187serine (C609T) and CYP1A2 exon 2 phenylalanine21leucine (C63G) polymorphisms do not play a significant role in breast cancer susceptibility in North Indian women. 21329464 2011
dbSNP: rs17861157
rs17861157
Entrez Id: 1544
Gene Symbol: CYP1A2
CYP1A2
CUI: C0202236
Disease:
Triglycerides measurement
0.700 GeneticVariation GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622 2012
dbSNP: rs17861157
rs17861157
Entrez Id: 1544
Gene Symbol: CYP1A2
CYP1A2
CUI: C1445957
Disease:
Serum total cholesterol measurement
0.700 GeneticVariation GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622 2012
dbSNP: rs201934979
rs201934979
Entrez Id: 1544
Gene Symbol: CYP1A2
CYP1A2
CUI: C0686347
Disease:
Tardive Dyskinesia
0.010 GeneticVariation BEFREE No significant differences in genotypes frequencies of the CYP2D6 C100T polymorphism were observed between patients with TD and without TD (Chi2=4.078, P>0.05), but patients with TD had a significant excess of the T allele compared with those without TD (Chi2=4.28, P<0.05). 16490169 2006
dbSNP: rs201934979
rs201934979
Entrez Id: 1544
Gene Symbol: CYP1A2
CYP1A2
CUI: C3714760
Disease:
Drug-induced tardive dyskinesia
0.010 GeneticVariation BEFREE The C100T polymorphism of the CYP2D6 gene and the C163A polymorphism of the CYP1A2 gene may be associated with neuroleptic drug-induced tardive dyskinesia in Chinese patients with schizophrenia. 16490169 2006
dbSNP: rs201934979
rs201934979
Entrez Id: 1544
Gene Symbol: CYP1A2
CYP1A2
CUI: C0036341
Disease:
Schizophrenia
0.010 GeneticVariation BEFREE The C100T polymorphism of the CYP2D6 gene and the C163A polymorphism of the CYP1A2 gene may be associated with neuroleptic drug-induced tardive dyskinesia in Chinese patients with schizophrenia. 16490169 2006
dbSNP: rs2069522
rs2069522
Entrez Id: 1544
Gene Symbol: CYP1A2
CYP1A2
CUI: C0009402
Disease:
Colorectal Carcinoma
0.010 GeneticVariation BEFREE There was a suggestion of increased risk, albeit insignificant after correction for multiple testing, of CRC for individuals homozygous for CYP1B1 rs162558 and heterozygous for CYP1A2 rs2069522 (odds ratio [OR] = 1.36, 95% confidence interval [CI]: 1.03-1.80 and OR = 1.34, 95% CI: 1.00-1.79 respectively). 17615053 2007
dbSNP: rs2069522
rs2069522
Entrez Id: 1544
Gene Symbol: CYP1A2
CYP1A2
CUI: C0006142
Disease:
Malignant neoplasm of breast
0.010 GeneticVariation BEFREE Our findings suggest that rs700519 and rs2069522 are associated with susceptibility to breast cancer</span> among the Han Chinese population and have a cumulative effect with three other identified SNPs. 25689428 2015
dbSNP: rs2069522
rs2069522
Entrez Id: 1544
Gene Symbol: CYP1A2
CYP1A2
CUI: C0678222
Disease:
Breast Carcinoma
0.010 GeneticVariation BEFREE Our findings suggest that rs700519 and rs2069522 are associated with susceptibility to breast cancer</span> among the Han Chinese population and have a cumulative effect with three other identified SNPs. 25689428 2015
dbSNP: rs2470890
rs2470890
Entrez Id: 1544
Gene Symbol: CYP1A2
CYP1A2
CUI: C0684249
Disease:
Carcinoma of lung
0.020 GeneticVariation BEFREE Previous published data on the association between CYP1A2 rs762551, rs2069514, rs2069526, and rs2470890 polymorphisms and lung cancer risk have not allowed a definite conclusion. 25081684 2014
dbSNP: rs2470890
rs2470890
Entrez Id: 1544
Gene Symbol: CYP1A2
CYP1A2
CUI: C1306460
Disease:
Primary malignant neoplasm of lung
0.020 GeneticVariation BEFREE Previous published data on the association between CYP1A2 rs762551, rs2069514, rs2069526, and rs2470890 polymorphisms and lung cancer risk have not allowed a definite conclusion. 25081684 2014
dbSNP: rs2470890
rs2470890
Entrez Id: 1544
Gene Symbol: CYP1A2
CYP1A2
CUI: C0242379
Disease:
Malignant neoplasm of lung
0.020 GeneticVariation BEFREE We found significant allele associations (rs2470890 and rs2422299) with lung cancer risk. 26987327 2016
dbSNP: rs2470890
rs2470890
Entrez Id: 1544
Gene Symbol: CYP1A2
CYP1A2
CUI: C0242379
Disease:
Malignant neoplasm of lung
0.020 GeneticVariation BEFREE Previous published data on the association between CYP1A2 rs762551, rs2069514, rs2069526, and rs2470890 polymorphisms and lung cancer risk have not allowed a definite conclusion. 25081684 2014
dbSNP: rs2470890
rs2470890
Entrez Id: 1544
Gene Symbol: CYP1A2
CYP1A2
CUI: C0684249
Disease:
Carcinoma of lung
0.020 GeneticVariation BEFREE We found significant allele associations (rs2470890 and rs2422299) with lung cancer risk. 26987327 2016
dbSNP: rs2470890
rs2470890
Entrez Id: 1544
Gene Symbol: CYP1A2
CYP1A2
CUI: C1306460
Disease:
Primary malignant neoplasm of lung
0.020 GeneticVariation BEFREE We found significant allele associations (rs2470890 and rs2422299) with lung cancer risk. 26987327 2016
dbSNP: rs2470890
rs2470890
Entrez Id: 1544
Gene Symbol: CYP1A2
CYP1A2
CUI: C3888516
Disease:
CYP1A2 polymorphism
0.010 GeneticVariation BEFREE This study has identified an association between the CYP1A2 polymorphism -1545C > T (rs2470890) and the occurrence of more severe clozapine side effects. 24555493 2014
dbSNP: rs2470890
rs2470890
Entrez Id: 1544
Gene Symbol: CYP1A2
CYP1A2
CUI: C0524620
Disease:
Metabolic Syndrome X
0.010 GeneticVariation BEFREE CYP rs2470890 allele 'C' increases the odds of T2DM by a factor of around 1.2 but decreases the odds of caffeine boosting T2DM of 1.7 by a factor of 0.77. rs2470890 showed an association with T2DM only when the interaction with coffee was considered, thereby setting an example of genetic activation by dietary changes associating with metabolic syndrome. 26588584 2016
dbSNP: rs2470890
rs2470890
Entrez Id: 1544
Gene Symbol: CYP1A2
CYP1A2
CUI: C0236734
Disease:
Caffeine related disorders
0.010 GeneticVariation BEFREE CYP rs2470890 allele 'C' increases the odds of T2DM by a factor of around 1.2 but decreases the odds of caffeine boosting T2DM of 1.7 by a factor of 0.77. rs2470890 showed an association with T2DM only when the interaction with coffee was considered, thereby setting an example of genetic activation by dietary changes associating with metabolic syndrome. 26588584 2016
dbSNP: rs2470890
rs2470890
Entrez Id: 1544
Gene Symbol: CYP1A2
CYP1A2
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent
0.010 GeneticVariation BEFREE CYP rs2470890 allele 'C' increases the odds of T2DM by a factor of around 1.2 but decreases the odds of caffeine boosting T2DM of 1.7 by a factor of 0.77. rs2470890 showed an association with T2DM only when the interaction with coffee was considered, thereby setting an example of genetic activation by dietary changes associating with metabolic syndrome. 26588584 2016
dbSNP: rs2470890
rs2470890
Entrez Id: 1544
Gene Symbol: CYP1A2
CYP1A2
CUI: C1269683
Disease:
Major Depressive Disorder
0.010 GeneticVariation BEFREE Our results suggest that the single-nucleotide polymorphism rs2470890 of CYP1A2 gene might be associated with treatment remission after VEN treatment in patients with MDD. 30875344 2019
dbSNP: rs2470890
rs2470890
Entrez Id: 1544
Gene Symbol: CYP1A2
CYP1A2
CUI: C0678222
Disease:
Breast Carcinoma
0.010 GeneticVariation BEFREE CYP1A2 rs2470890 was significantly associated with the prognosis of patients with breast cancer and could serve as an independent impact factor of prognosis of breast carcinoma. 28418906 2017
dbSNP: rs2470890
rs2470890
Entrez Id: 1544
Gene Symbol: CYP1A2
CYP1A2
CUI: C0030567
Disease:
Parkinson Disease
0.010 GeneticVariation BEFREE CYP1A2 polymorphisms were not associated with PD risk; however, the coffee-PD association was strongest among subjects homozygous for either variant allele rs762551 (P(interaction) = 0.05) or rs2470890 (P(interaction) = 0.04). 21281405 2011
dbSNP: rs2470890
rs2470890
Entrez Id: 1544
Gene Symbol: CYP1A2
CYP1A2
CUI: C0006142
Disease:
Malignant neoplasm of breast
0.010 GeneticVariation BEFREE CYP1A2 rs2470890 was significantly associated with the prognosis of patients with breast cancer and could serve as an independent impact factor of prognosis of breast carcinoma. 28418906 2017
dbSNP: rs2470890
rs2470890
Entrez Id: 1544
Gene Symbol: CYP1A2
CYP1A2
CUI: C0009402
Disease:
Colorectal Carcinoma
0.010 GeneticVariation BEFREE Through an association study based on 1,023 cases and 1,121 controls, we examined the influence on CRC risk of environmental factors coanalyzed with combinations of six single nucleotide polymorphisms located in cytochrome P450 genes (c.-163A>C and c.1548T>C in CYP1A2, g.-1293G>C and g.-1053C>T in CYP2E1, c.1294C>G in CYP1B1, and c.430C>T in CYP2C9). 17627011 2007