rs121913059, CFH

N. diseases: 16
Disease: C3 glomerulopathy ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
C3 glomerulopathy
CUI: C4087273
Disease: C3 glomerulopathy
0.010 GeneticVariation BEFREE The complement factor H (FH) mutation R1210C, which was described in association with atypical hemolytic uremic syndrome (aHUS), also confers high risk of age-related macular degeneration (AMD) and associates with C3 glomerulopathy (C3G). 26376859 2016