Disease: Idiopathic Membranous Glomerulonephritis ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Idiopathic Membranous Glomerulonephritis
CUI: C0086445
Disease: Idiopathic Membranous Glomerulonephritis
0.040 GeneticVariation BEFREE Our pooled analysis showed a significant association between rs2187668-(A) allele and iMN susceptibility, and the intervention of this mutation might bring new therapeutic strategy for iMN. 30383665 2018
Idiopathic Membranous Glomerulonephritis
CUI: C0086445
Disease: Idiopathic Membranous Glomerulonephritis
0.040 GeneticVariation BEFREE Allelic frequency distributions for SNP rs2187668 within HLA-DQA1 were significantly different between the iMN and control groups. 28849274 2018
Idiopathic Membranous Glomerulonephritis
CUI: C0086445
Disease: Idiopathic Membranous Glomerulonephritis
0.040 GeneticVariation BEFREE Even under dominant model, the two SNPs were still significantly associated with IMN (P = 3.50×10-3 for rs28383345 and P = 6.55×10-5 for rs2187668). 28685717 2017
Idiopathic Membranous Glomerulonephritis
CUI: C0086445
Disease: Idiopathic Membranous Glomerulonephritis
0.040 GeneticVariation BEFREE We believe this will be a valuable technique for determining the genotype of rs2187668 and rs4664308 and for assessing individual susceptibility to IMN. 23194743 2013