Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2032582
rs2032582
ABCB1
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
ABCB1
0.020 GeneticVariation BEFREE Patients with NS carrying homozygous mutants of single nucleotide polymorphism (SNP) G2677T/A are prone to develop SRNS. 21460357

2011