rs387906536, LYZ

N. diseases: 6
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Amyloidosis
CUI: C0002726
Disease: Amyloidosis
0.030 GeneticVariation BEFREE Here we report a lysozyme amyloidosis family with variant lysozyme p.Trp82Arg in a Chinese family. 31395023 2019
Amyloidosis
CUI: C0002726
Disease: Amyloidosis
0.030 GeneticVariation BEFREE The literature review highlights that hereditary ALys with the p.Trp82Arg variant is frequent in patients coming from Piedmont (Italy). 28963698 2017
Amyloidosis
CUI: C0002726
Disease: Amyloidosis
0.030 GeneticVariation BEFREE Clinical manifestations and organ involvement of nine affected members of a new family with the p.</span>Trp82Arg ALys variant were recorded. 25217048 2014