rs387906536, LYZ

N. diseases: 6
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Amyloid nephropathy
CUI: C0268382
Disease: Amyloid nephropathy
0.010 GeneticVariation BEFREE Hereditary renal amyloidosis with a variant lysozyme p.Trp82Arg in a Chinese family: case report and literature review. 31395023 2019