Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1048943
rs1048943
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
0.050 GeneticVariation BEFREE <b>Conclusion.</b> This meta-analysis revealed a clear association between rs104</span>8943 and rs4646903 polymorphisms of the <i>CYP1A1</i> gene but not between CYP1B1 rs10012, rs162549, rs1800440, and rs2551188 polymorphisms and the risk of PCa. 30765615

2019

dbSNP: rs1048943
rs1048943
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.050 GeneticVariation BEFREE <b>Conclusion.</b> This meta-analysis revealed a clear association between rs104</span>8943 and rs4646903 polymorphisms of the <i>CYP1A1</i> gene but not between CYP1B1 rs10012, rs162549, rs1800440, and rs2551188 polymorphisms and the risk of PCa. 30765615

2019

dbSNP: rs1048943
rs1048943
CUI: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix
0.090 GeneticVariation BEFREE (2) rs1048943 (CYP1A1 A4889G) showed the strongest association with cervical cancer in the allele effect model (1.83[1.57, 2.13]); in addition, rs1048943 (CYP1A1 A4889G) had a very strong association in the dominant and recessive effect model. 25928231

2015

dbSNP: rs1048943
rs1048943
CUI: C0302592
Disease: Cervix carcinoma
Cervix carcinoma
0.090 GeneticVariation BEFREE (2) rs1048943 (CYP1A1 A4889G) showed the strongest association with cervical cancer in the allele effect model (1.83[1.57, 2.13]); in addition, rs1048943 (CYP1A1 A4889G) had a very strong association in the dominant and recessive effect model. 25928231

2015

dbSNP: rs1048943
rs1048943
CUI: C4048328
Disease: cervical cancer
cervical cancer
0.090 GeneticVariation BEFREE (2) rs1048943 (CYP1A1 A4889G) showed the strongest association with cervical cancer in the allele effect model (1.83[1.57, 2.13]); in addition, rs1048943 (CYP1A1 A4889G) had a very strong association in the dominant and recessive effect model. 25928231

2015

dbSNP: rs1048943
rs1048943
CUI: C0020473
Disease: Hyperlipidemia
Hyperlipidemia
0.010 GeneticVariation BEFREE Hyperlipidemia could modulate the effect of CYP1A1 rs1048943 on the periodontal status of GAgP. 31032950

2019

dbSNP: rs1048943
rs1048943
CUI: C0919267
Disease: ovarian neoplasm
ovarian neoplasm
0.030 GeneticVariation BEFREE Ile462Val status seems to represent a meaningful risk factor for ovarian cancer in Caucasians. 22733497

2012

dbSNP: rs1048943
rs1048943
CUI: C4721610
Disease: Carcinoma, Ovarian Epithelial
Carcinoma, Ovarian Epithelial
0.020 GeneticVariation BEFREE Ile462Val status seems to represent a meaningful risk factor for ovarian cancer in Caucasians. 22733497

2012

dbSNP: rs1048943
rs1048943
CUI: C1140680
Disease: Malignant neoplasm of ovary
Malignant neoplasm of ovary
0.020 GeneticVariation BEFREE Ile462Val status seems to represent a meaningful risk factor for ovarian cancer in Caucasians. 22733497

2012

dbSNP: rs1048943
rs1048943
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
Non-Small Cell Lung Carcinoma
0.040 GeneticVariation BEFREE A case-control study was carried out on 1,040 nonsmall cell lung cancer (NSCLC) cases and 784 controls to investigate three CYP1A1 variants, CYP1A1*2A (rs4646903; thymidine to cytosine substitution at nucleotide 3801 (3801T>C)), CYP1A1*2C (rs1048943; 2455A>G; substitution of isoleucine 462 with valine (exon 7)) and CYP1A1*4 (rs1799814; 2453C>A; substitution of threonine 461 with asparagine (exon 7)) using PCR restriction fragment length polymorphism methods. 19608585

2010

dbSNP: rs1048943
rs1048943
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.030 GeneticVariation BEFREE A great number of studies regarding the association between MspI and Ile462Val polymorphisms in the CYP1A1 gene and gastric cancer have been published. 22359202

2012

dbSNP: rs1048943
rs1048943
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.030 GeneticVariation BEFREE A great number of studies regarding the association between MspI and Ile462Val polymorphisms in the CYP1A1 gene and gastric cancer have been published. 22359202

2012

dbSNP: rs1048943
rs1048943
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.070 GeneticVariation BEFREE A semi-quantitative food frequency questionnaire was used to assess the dietary intake of six flavonoid subclasses (flavonols, flavones, flavanones, flavan-3-ols, anthocyanidins, and isoflavones) in 923 patients with colorectal cancer and 1,846 controls; furthermore, CYP1A1 genetic variants (rs4646903 and rs1048943) were genotyped. 28273931

2017

dbSNP: rs1048943
rs1048943
Malignant neoplasm of colon and/or rectum
0.060 GeneticVariation BEFREE A semi-quantitative food frequency questionnaire was used to assess the dietary intake of six flavonoid subclasses (flavonols, flavones, flavanones, flavan-3-ols, anthocyanidins, and isoflavones) in 923 patients with colorectal cancer and 1,846 controls; furthermore, CYP1A1 genetic variants (rs4646903 and rs1048943) were genotyped. 28273931

2017

dbSNP: rs1048943
rs1048943
CUI: C0598608
Disease: Hyperhomocysteinemia
Hyperhomocysteinemia
0.010 GeneticVariation BEFREE All subjects were genotyped for 13 polymorphic variants in the genes of xenobiotics detoxification CYP1A1 (rs2606345, rs4646903, and rs1048943), GSTM1 (Ins/del), GSTT1 (Ins/del), ABCB1 rs1045642); immune and inflammation response IL-6 (rs1800795), TNF-a (rs1800629), MBL2 (rs7096206), CCR5 (rs333), NOS3 (rs1799983), angiotensin-converting enzyme ACE (rs4340), and occlusive vascular disease/hyperhomocysteinemia MTHFR (rs1801133). 23107763

2013

dbSNP: rs1048943
rs1048943
CUI: C0153381
Disease: Malignant neoplasm of mouth
Malignant neoplasm of mouth
0.030 GeneticVariation BEFREE Among these 14 variants, 9 variants were reported to be significantly associated with the risk of oral cancer (CYP1A1-MspI, CYP2E1-RsaI/PstI, MTHFR-C677T, p73-G4C14-to-A4T14, XRCC1-Arg194Trp, CYP1A1-Ile462Val, GSTM1-±, and NAT2 slow vs rapid). 24102947

2014

dbSNP: rs1048943
rs1048943
CUI: C0220641
Disease: Lip and Oral Cavity Carcinoma
Lip and Oral Cavity Carcinoma
0.030 GeneticVariation BEFREE Among these 14 variants, 9 variants were reported to be significantly associated with the risk of oral cancer (CYP1A1-MspI, CYP2E1-RsaI/PstI, MTHFR-C677T, p73-G4C14-to-A4T14, XRCC1-Arg194Trp, CYP1A1-Ile462Val, GSTM1-±, and NAT2 slow vs rapid). 24102947

2014

dbSNP: rs1048943
rs1048943
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung
0.100 GeneticVariation BEFREE An elevated risk of lung cancer was observed among individuals with the MspI CC (OR=1.7, 95 CI=0.9-3.3) and Ile(462)Val ValVal genotypes (OR=2.8, 95 CI=1.1-7.6). 15953982

2005

dbSNP: rs1048943
rs1048943
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung
0.100 GeneticVariation BEFREE An elevated risk of lung cancer was observed among individuals with the MspI CC (OR=1.7, 95 CI=0.9-3.3) and Ile(462)Val ValVal genotypes (OR=2.8, 95 CI=1.1-7.6). 15953982

2005

dbSNP: rs1048943
rs1048943
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung
0.100 GeneticVariation BEFREE An elevated risk of lung cancer was observed among individuals with the MspI CC (OR=1.7, 95 CI=0.9-3.3) and Ile(462)Val ValVal genotypes (OR=2.8, 95 CI=1.1-7.6). 15953982

2005

dbSNP: rs1048943
rs1048943
CUI: C1691215
Disease: Penile hypospadias
Penile hypospadias
0.010 GeneticVariation BEFREE Analysis of the distributions of SNPs in CYP1A1 and CYP17A1 genes showed that the mutant genotype CC (OR = 4.87) of CYP1A1 rs1048943, and mutant genotype CC (OR = 5.82), recessive genotype AC + CC (OR = 2.17) and allele C (OR = 1.77) of CYP17A1 rs4919686 significantly increased the risk of HS. 30858503

2019

dbSNP: rs1048943
rs1048943
CUI: C0848558
Disease: Hypospadias
Hypospadias
0.010 GeneticVariation BEFREE Analysis of the distributions of SNPs in CYP1A1 and CYP17A1 genes showed that the mutant genotype CC (OR = 4.87) of CYP1A1 rs1048943, and mutant genotype CC (OR = 5.82), recessive genotype AC + CC (OR = 2.17) and allele C (OR = 1.77) of CYP17A1 rs4919686 significantly increased the risk of HS. 30858503

2019

dbSNP: rs1048943
rs1048943
CUI: C0001342
Disease: Acute periodontitis
Acute periodontitis
0.010 GeneticVariation BEFREE Association of CYP1A1 rs1048943 variant with aggressive periodontitis and its interaction with hyperlipidemia on the periodontal status. 31032950

2019

dbSNP: rs1048943
rs1048943
CUI: C0031106
Disease: Aggressive Periodontitis
Aggressive Periodontitis
0.010 GeneticVariation BEFREE Association of CYP1A1 rs1048943 variant with aggressive periodontitis and its interaction with hyperlipidemia on the periodontal status. 31032950

2019

dbSNP: rs1048943
rs1048943
CUI: C4048328
Disease: cervical cancer
cervical cancer
0.090 GeneticVariation BEFREE Association of CYP1A1 gene variants rs4646903 (T>C) and rs1048943 (A>G) with cervical cancer in a North Indian population. 24657182

2014