rs1045642, ABCB1

N. diseases: 214
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Major Depressive Disorder
CUI: C1269683
Disease: Major Depressive Disorder
0.070 GeneticVariation BEFREE MDD is associated with the rs2032582 (<i>G2677T</i>) and rs1128503 (<i>C1236T</i>) single-nucleotide polymorphisms (SNPs) of <i>ABCB1</i> but not with rs1045642, rs2032583, rs2235040, and rs2235015. 31333472 2019
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
0.100 GeneticVariation BEFREE We observed difference in SNPs in MDR1 gene C3435T p</span>olymorphism between breast cancer patients and healthy controls (chi(2) = 8.66, df = 2, p = 0.013). 17560460 2007
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
0.100 GeneticVariation BEFREE We observed difference in SNPs in MDR1 gene C3435T p</span>olymorphism between breast cancer patients and healthy controls (chi(2) = 8.66, df = 2, p = 0.013). 17560460 2007
Leukemia, Myelocytic, Acute
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
0.040 GeneticVariation BEFREE C3435T polymorphism of the MDR1 gene is not associated with P-glycoprotein function of leukemic blasts and clinical outcome in patients with acute myeloid leukemia. 18272218 2008
Cholangiocarcinoma
CUI: C0206698
Disease: Cholangiocarcinoma
0.010 GeneticVariation BEFREE C3435T genotype was an independent predictive factor of good response in breast (response >50 %, i.e., Sataloff T-A and T-B): OR: 4.6 (95 % CI: 1.3-16.1), p = 0.015, for TT patients versus CT and CC patients. 23666532 2013
Leukopenia
CUI: C0023530
Disease: Leukopenia
0.100 GeneticVariation BEFREE C3435T polymorphisms of ABCB1 might be able to predict severe amrubicin-induced neutropenia. 24982363 2014
Neutropenia
CUI: C0027947
Disease: Neutropenia
0.080 GeneticVariation BEFREE C3435T polymorphisms of ABCB1 might be able to predict severe amrubicin-induced neutropenia. 24982363 2014
Childhood Acute Lymphoblastic Leukemia
0.100 GeneticVariation BEFREE C3435T and C1236T MDR1 polymorphism are significantly associated with the high-risk group (OR=2.6, 95%CI=1.164-5.808; P=0.028 and OR=2.231, 95%CI=1.068-4.659; p=0.047, respectively), indicating that both may be candidates for molecular markers in the high-risk group of ALL. 25854371 2015
Epilepsy
CUI: C0014544
Disease: Epilepsy
0.100 GeneticVariation BEFREE C3435T polymorphism of MDR1 gene was analysed by the high resolution melting technique in a group of patients with drug-resistant (n = 106) and drug-responsive epilepsy (n = 67), as well as in non-epileptic children (n = 98) hospitalised at the Department of Neurology, Polish Mother's Memorial Hospital in Lodz. 27391700 2016
Ulcerative Colitis
CUI: C0009324
Disease: Ulcerative Colitis
0.100 GeneticVariation BEFREE A meta-analysis of 9 association studies of C34</span>35T showed a significant association of the 3435T allele with UC (OR 1.12; 95% CI 1.02-1.23; P = 0.013) but not with CD. 16633048 2006
Inflammatory Bowel Diseases
CUI: C0021390
Disease: Inflammatory Bowel Diseases
0.100 GeneticVariation BEFREE A meta-analysis was carried out of our results and those from 8 previously published association studies of the C3435T variant in inflammatory bowel disease. 16633048 2006
Epilepsy
CUI: C0014544
Disease: Epilepsy
0.100 GeneticVariation BEFREE A meta-analysis was conducted to assess the role of the C3435T polymorphism in drug-resistance in epilepsy. 24794827 2014
Sporadic Breast Carcinoma
CUI: C1336076
Disease: Sporadic Breast Carcinoma
0.010 GeneticVariation BEFREE A polymorphism C3435T of the MDR-1 gene associated with smoking or high body mass index increases the risk of sporadic breast cancer in women. 17549370 2007
Parkinsonian Disorders
CUI: C0242422
Disease: Parkinsonian Disorders
0.020 GeneticVariation BEFREE A significant association between patients with parkinsonism exposed to pesticides and C3435T polymorphism of the MDR1 gene was found. 12724617 2003
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
0.100 GeneticVariation BEFREE A significant association of MDR1 C3435T with CD was observed (CC vs (CT + TT): P = 0.007; OR [95% CI] = 1.58 [1.12-2.23]). 16374256 2006
Major Depressive Disorder
CUI: C1269683
Disease: Major Depressive Disorder
0.070 GeneticVariation BEFREE A significant protection for MDD males carrying the T allele was observed (C1236T: odds ratio (OR)=0.360, 95% confidence interval [CI]: [0.140-0.950], p=0.022; C3435T: OR=0.306, 95% CI: [0.096-0.980], p=0.042; and G2677TA: OR=0.300, 95% CI: [0.100-0.870], p=0.013). 24200053 2014
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
0.100 GeneticVariation BEFREE A statistical association was observed between p53 codon 72 polymorphism and family history of breast cancer in both groups, as well as between MDR1 C3435T and smoking habits in cases (P<0.05).Gene polymorphisms vary by regions. 19885596 2009
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
0.100 GeneticVariation BEFREE A statistical association was observed between p53 codon 72 polymorphism and family history of breast cancer in both groups, as well as between MDR1 C3435T and smoking habits in cases (P<0.05).Gene polymorphisms vary by regions. 19885596 2009
Mixed cryoglobulinemia
CUI: C0543697
Disease: Mixed cryoglobulinemia
0.010 GeneticVariation BEFREE ABCB1 (gene encoding P-glycoprotein) 3435C>T SNP was associated with MC presence (p = 0.034): related to T allele carriers (CC vs CT/TT), we reached a p-value of 0.013. 28453396 2017
Epilepsy
CUI: C0014544
Disease: Epilepsy
0.100 GeneticVariation BEFREE ABCB1 3435C>T was genotyped in 746 Han Chinese patients with epilepsy and 179 controls. 17521963 2007
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
0.040 GeneticVariation BEFREE ABCB1 C3435T polymorphism and response to clopidogrel treatment in coronary artery disease (CAD) patients: a meta-analysis. 23056288 2012
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
0.040 GeneticVariation BEFREE ABCB1 C3435T polymorphism and the risk of coronary heart disease: a meta-analysis. 24328528 2014
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
0.020 GeneticVariation BEFREE ABCB1 C3435T polymorphism and the risk of coronary heart disease: a meta-analysis. 24328528 2014
Myocardial Ischemia
CUI: C0151744
Disease: Myocardial Ischemia
0.010 GeneticVariation BEFREE ABCB1 C3435T polymorphism and the risk of ischemic heart disease: a meta-analysis. 25118983 2014
Acute leukemia
CUI: C0085669
Disease: Acute leukemia
0.030 GeneticVariation BEFREE ABCB1 3435C > T polymorphisms may be associated with susceptibility to acute leukemia, and ABCB1 polymorphisms might be a sensitive indicator for predicting efficacy of MTX therapy in the treatment of acute leukemia. 25921280 2015