Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2032582
rs2032582
0.040 GeneticVariation BEFREE In terms of pathological characteristics, the <i>ABCC1</i> SNP rs35628 and the <i>ABCB1</i> SNP rs2032582 were significantly associated with tumor size, the <i>ABCC2</i> SNP rs2273697 was significantly associated with estrogen receptor status, and the <i>ABCG2</i> SNP rs2231142 was significantly associated with axillary lymph node status. 31391850

2019

dbSNP: rs1045642
rs1045642
0.040 GeneticVariation BEFREE Following meta-analysis, significant associations were seen for six tumor variants (mutant TP53 and PIK3CA, copy number gain of ERBB2/HER2, CCND1 and FGF3, and chromosomal instability/ploidy) and seven germline polymorphisms: ERCC1 rs3212986, ERCC2 rs1799793, TP53 rs1042522, MDM2 rs2279744, TYMS rs34743033, ABCB1 rs1045642 and MTHFR rs1801133. 25214541

2015

dbSNP: rs2032582
rs2032582
0.040 GeneticVariation BEFREE Significant associations of rs2032582 SNP with tumor size, negative HER-2/neu status, and family history of breast carcinoma were found. 23093106

2012

dbSNP: rs1045642
rs1045642
0.040 GeneticVariation BEFREE The G2677T and C3435T polymorphisms were studied and immunohistochemical analysis of the tumor and adjacent normal tissue was performed. 19192650

2009

dbSNP: rs2032582
rs2032582
0.040 GeneticVariation BEFREE The G2677T and C3435T polymorphisms were studied and immunohistochemical analysis of the tumor and adjacent normal tissue was performed. 19192650

2009

dbSNP: rs1045642
rs1045642
0.040 GeneticVariation BEFREE We analyzed the C3435T SNP in the MDR1 gene which is associated with altered cellular drug uptake in matched tumor and normal tissues of 45 patients suffering from colorectal carcinoma. 12894567

2003

dbSNP: rs1045642
rs1045642
0.040 GeneticVariation BEFREE The estimated allele frequencies of functional polymorphisms in(of) exon 21 (2677 G>T, Ala893Ser) and exon 26(3435 C>T, Ilel 142I1e) of the MDR] gene were 0.42 and 0.46 in the controls and 0.54 (p=0.035) and 0.60 (p=0.017) in the MSI-H tumors. 11980438

2002

dbSNP: rs2032582
rs2032582
0.040 GeneticVariation BEFREE The estimated allele frequencies of functional polymorphisms in(of) exon 21 (2677 G>T, Ala893Ser) and exon 26(3435 C>T, Ilel 142I1e) of the MDR] gene were 0.42 and 0.46 in the controls and 0.54 (p=0.035) and 0.60 (p=0.017) in the MSI-H tumors. 11980438

2002

dbSNP: rs1128503
rs1128503
0.020 GeneticVariation BEFREE CC and TC+TT genotype patients with C1236T loci showed statistically significant differences in tumor size stratification (χ=4.006, P=0.045). 30779721

2019

dbSNP: rs1128503
rs1128503
0.020 GeneticVariation BEFREE The tumour response to docetaxel was significantly influenced by the SNP C1236T of ABCB1 gene coding for the P-gp. 30637776

2019

dbSNP: rs201661522
rs201661522
0.010 GeneticVariation BEFREE It is approved for first-line treatment of patients with advanced non-small cell lung cancer (NSCLC) whose tumors have EGFR exon 19 deletions or exon 21 L858R mutations, and for patients with T790M-positive advanced NSCLC whose disease has progressed on or after EGFR-TKI therapy. 30875094

2019