Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
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: rs762551
rs762551
Entrez Id: 1544
Gene Symbol: CYP1A2
CYP1A2
CUI: C0236734
Disease:
Caffeine related disorders
0.100 GeneticVariation BEFREE We also evaluated patient genotype in the caffeine metabolism related single nucleotide polymorphism rs762551. 30179617 2019
dbSNP: rs762551
rs762551
Entrez Id: 1544
Gene Symbol: CYP1A2
CYP1A2
CUI: C0236734
Disease:
Caffeine related disorders
0.100 GeneticVariation BEFREE This study aimed to examine whether functional single nucleotide polymorphisms (SNPs) in 1976T > C (ADORA2A; rs5751876) and -163C > A (CYP1A2; rs762551) influence the effect of caffeine on the postprandial glucose (GLU) response to a carbohydrate meal. 31324842 2019
dbSNP: rs762551
rs762551
Entrez Id: 1544
Gene Symbol: CYP1A2
CYP1A2
CUI: C0236734
Disease:
Caffeine related disorders
0.100 GeneticVariation BEFREE In stratified analysis, a statistical significance within the caffeinated group was observed for the change in systolic BP in the stratum of CYP1A2 polymorphism with daily caffeine consumption ≤90 mg/day: change in systolic BP in the CYP1A2 rs762551 CC group (mean ± SD = 11.8 ± 5.9) was higher than that in the AA/CA group (4.1 ± 5.5). 30773300 2019
dbSNP: rs762551
rs762551
Entrez Id: 1544
Gene Symbol: CYP1A2
CYP1A2
CUI: C0236734
Disease:
Caffeine related disorders
0.100 GeneticVariation BEFREE Participants were measured twice in a metabolic chamber for a day, four weeks apart, with outcomes including 22 h EE (8:30-6:30), substrate utilization from the respiratory quotient (RQ), plasma caffeine levels (16:00), and genotyping for the single-nucleotide polymorphism (SNP) rs762551. 31694152 2019
dbSNP: rs762551
rs762551
Entrez Id: 1544
Gene Symbol: CYP1A2
CYP1A2
CUI: C0236734
Disease:
Caffeine related disorders
0.100 GeneticVariation BEFREE Spot urine samples obtained 6 hours following 200-mg caffeine administration were used to determine caffeine metabolite ratios (CMRs); blood samples were used to determine CYP1A2*1F (rs762551) and CYP1A2*1C (rs2069514) polymorphisms and the hormonal profile (estradiol, progesterone, and luteinizing and follicle-stimulating hormones) at EFP, LFP, and LP. 30591530 2019
dbSNP: rs762551
rs762551
Entrez Id: 1544
Gene Symbol: CYP1A2
CYP1A2
CUI: C0236734
Disease:
Caffeine related disorders
0.100 GeneticVariation BEFREE The effects of caffeine on basketball performance were established according to players' CYP1A2 genotype (rs762551): AA homozygotes (n = 10) and C-allele carriers (n = 9). 29668752 2018
dbSNP: rs762551
rs762551
Entrez Id: 1544
Gene Symbol: CYP1A2
CYP1A2
CUI: C0236734
Disease:
Caffeine related disorders
0.100 GeneticVariation BEFREE Our findings do not support the hypothesis of an interaction between the GRIN2A-rs4998386 or CYP1A2-rs762551 polymorphism and caffeine intake in determining PD risk. 29318639 2018
dbSNP: rs762551
rs762551
Entrez Id: 1544
Gene Symbol: CYP1A2
CYP1A2
CUI: C0236734
Disease:
Caffeine related disorders
0.100 GeneticVariation BEFREE Specifically, the rs762551 SNP in the CYP1A2 gene has been demonstrated to influence caffeine metabolism, with carriers of the C allele considered to be of a 'slow' metaboliser phenotype. 29569539 2018
dbSNP: rs762551
rs762551
Entrez Id: 1544
Gene Symbol: CYP1A2
CYP1A2
CUI: C0236734
Disease:
Caffeine related disorders
0.100 GeneticVariation BEFREE The association between the single nucleotide polymorphism rs762551 in the cytochrome P450 family 1, subfamily A2 gene (CYP1A2) and caffeine consumption remains controversial. 27173183 2016
dbSNP: rs762551
rs762551
Entrez Id: 1544
Gene Symbol: CYP1A2
CYP1A2
CUI: C0236734
Disease:
Caffeine related disorders
0.100 GeneticVariation BEFREE The observed increased risk of PD among female but not male carriers of the rs762551 polymorphism of CYP1A2 and the interactions of caffeine with ESR1 rs3798577 and ESR2 rs1255998 may provide clues to explain the relationship between gender, caffeine intake, estrogen status and risk of PD and need to be replicated. 20304699 2010
dbSNP: rs762551
rs762551
Entrez Id: 1544
Gene Symbol: CYP1A2
CYP1A2
CUI: C0236734
Disease:
Caffeine related disorders
0.100 GeneticVariation BEFREE We collected information on lifetime coffee drinking and we studied two genes: ADORA2A, which encodes the major receptor activity of caffeine in the brain (variants rs5751876 and rs3032740), and CYP1A2, which encodes the major rate-limiting step of caffeine metabolism (variants rs35694136 and rs762551). 18759349 2008
dbSNP: rs762551
rs762551
Entrez Id: 1544
Gene Symbol: CYP1A2
CYP1A2
CUI: C1306459
Disease:
Primary malignant neoplasm
0.060 GeneticVariation BEFREE The meta-analysis of 62 studies on rs762551, reported an OR of 1.03 (95% CI, 0.96-1.12) for overall cancer (P for heterogeneity < 0.01; I(2) = 50.4%). 26865042 2016
dbSNP: rs762551
rs762551
Entrez Id: 1544
Gene Symbol: CYP1A2
CYP1A2
CUI: C0006826
Disease:
Malignant Neoplasms
0.060 GeneticVariation BEFREE The meta-analysis of 62 studies on rs762551, reported an OR of 1.03 (95% CI, 0.96-1.12) for overall cancer (P for heterogeneity < 0.01; I(2) = 50.4%). 26865042 2016
dbSNP: rs762551
rs762551
Entrez Id: 1544
Gene Symbol: CYP1A2
CYP1A2
CUI: C0006826
Disease:
Malignant Neoplasms
0.060 GeneticVariation BEFREE The previously published data on the association between CYP1A2*1C (rs2069514) and CYP1A2*1F (rs762551) polymorphisms and cancer risk have remained controversial. 25472037 2015
dbSNP: rs762551
rs762551
Entrez Id: 1544
Gene Symbol: CYP1A2
CYP1A2
CUI: C1306459
Disease:
Primary malignant neoplasm
0.060 GeneticVariation BEFREE The previously published data on the association between CYP1A2*1C (rs2069514) and CYP1A2*1F (rs762551) polymorphisms and cancer risk have remained controversial. 25472037 2015
dbSNP: rs762551
rs762551
Entrez Id: 1544
Gene Symbol: CYP1A2
CYP1A2
CUI: C1306459
Disease:
Primary malignant neoplasm
0.060 GeneticVariation BEFREE Emerging evidence showed that the common polymorphism (CYP1A2 1F, rs762551 C→A) in the promoter region of the CYP1A2 gene might be associated with susceptibility to cancer in humans. 23628800 2013
dbSNP: rs762551
rs762551
Entrez Id: 1544
Gene Symbol: CYP1A2
CYP1A2
CUI: C0006826
Disease:
Malignant Neoplasms
0.060 GeneticVariation BEFREE Emerging evidence showed that the common polymorphism (CYP1A2 1F, rs762551 C→A) in the promoter region of the CYP1A2 gene might be associated with susceptibility to cancer in humans. 23628800 2013
dbSNP: rs762551
rs762551
Entrez Id: 1544
Gene Symbol: CYP1A2
CYP1A2
CUI: C0006826
Disease:
Malignant Neoplasms
0.060 GeneticVariation BEFREE These results suggest that the rs3569413 polymorphism of the CYP1A2 gene is associated with an increased risk of lung cancer and the rs762551 polymorphism of the CYP1A2 gene might be a potential biomarker for the risk of cancer among Caucasians. 23462460 2013
dbSNP: rs762551
rs762551
Entrez Id: 1544
Gene Symbol: CYP1A2
CYP1A2
CUI: C1306459
Disease:
Primary malignant neoplasm
0.060 GeneticVariation BEFREE These results suggest that the rs3569413 polymorphism of the CYP1A2 gene is associated with an increased risk of lung cancer and the rs762551 polymorphism of the CYP1A2 gene might be a potential biomarker for the risk of cancer among Caucasians. 23462460 2013
dbSNP: rs762551
rs762551
Entrez Id: 1544
Gene Symbol: CYP1A2
CYP1A2
CUI: C0006826
Disease:
Malignant Neoplasms
0.060 GeneticVariation BEFREE We studied the interactions of the CYP1A2 functional variants -3860G/A(rs2069514),-2467T/delT(rs3569413),-163C/A(rs762551)] with occupational/environmental carcinogenic exposures in the development of lung cancer in a case-control study nested in the Danish prospective cohort "Diet, Cancer and Health." 22749033 2012
dbSNP: rs762551
rs762551
Entrez Id: 1544
Gene Symbol: CYP1A2
CYP1A2
CUI: C1306459
Disease:
Primary malignant neoplasm
0.060 GeneticVariation BEFREE Genetic polymorphism (rs762551A>C) in gene encoding cytochrome P450 1A2 (CYP1A2) has been shown to influence the inducibility of CYP1A2 expression and thus might be associated with risk of several types of human cancer. 23157985 2012
dbSNP: rs762551
rs762551
Entrez Id: 1544
Gene Symbol: CYP1A2
CYP1A2
CUI: C1306459
Disease:
Primary malignant neoplasm
0.060 GeneticVariation BEFREE These results suggested that CYP1A2 rs762551 polymorphism is likely to be associated with susceptibility to cancer in Caucasians. 23157985 2012
dbSNP: rs762551
rs762551
Entrez Id: 1544
Gene Symbol: CYP1A2
CYP1A2
CUI: C1306459
Disease:
Primary malignant neoplasm
0.060 GeneticVariation BEFREE We studied the interactions of the CYP1A2 functional variants -3860G/A(rs2069514),-2467T/delT(rs3569413),-163C/A(rs762551)] with occupational/environmental carcinogenic exposures in the development of lung cancer in a case-control study nested in the Danish prospective cohort "Diet, Cancer and Health." 22749033 2012