Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Nephrosis, congenital
CUI: C3501848
Disease: Nephrosis, congenital
0.010 GeneticVariation BEFREE In contrast, patients with LAMB2 missense mutations, such as R246Q, can have less severe extrarenal defects but still exhibit congenital nephrotic syndrome. 21511833 2011