Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1128503
rs1128503
0.020 GeneticVariation BEFREE ABCB1 C1236T, ABCB1 G2677 T/A genotype and BMI are probably the factors influencing the clinical efficacy of TAC in treating patients with NS. 29615122

2018

dbSNP: rs1045642
rs1045642
0.020 GeneticVariation BEFREE The frequencies of MDR1 G2677T/A GT, GA, TT+AA genotypes or T allele, MDR1 C3435T TT genotype, and T allele genotype frequencies were significantly increased in NS group. 23994685

2013

dbSNP: rs2032582
rs2032582
0.020 GeneticVariation BEFREE The frequencies of MDR1 G2677T/A GT, GA, TT+AA genotypes or T allele, MDR1 C3435T TT genotype, and T allele genotype frequencies were significantly increased in NS group. 23994685

2013

dbSNP: rs1045642
rs1045642
0.020 GeneticVariation BEFREE The synergistic effect of mutant genotypes of SNPs G2677T/A and C3435T in different combinations increase the risk of developing steroid resistance in patients with NS. 21460357

2011

dbSNP: rs1128503
rs1128503
0.020 GeneticVariation BEFREE We undertook this study to examine the distribution of three most frequent MDR-1 exonic polymorphisms G3435C, G2677T/A and C1236T in patients with NS and control children to investigate their usefulness as markers of responsiveness of the disease to steroids. 21460357

2011

dbSNP: rs2032582
rs2032582
0.020 GeneticVariation BEFREE Patients with NS carrying homozygous mutants of single nucleotide polymorphism (SNP) G2677T/A are prone to develop SRNS. 21460357

2011