rs121913547, LYZ

N. diseases: 7
Disease: Amyloidosis, Familial ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Amyloidosis, Familial
CUI: C0740340
Disease: Amyloidosis, Familial
0.010 GeneticVariation BEFREE A non-natural variant of human lysozyme (I59T) mimics the in vitro behaviour of the I56T variant that is responsible for a form of familial amyloidosis. 20382744 2010