rs121913547, LYZ

N. diseases: 7
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Amyloidosis, familial visceral
CUI: C0268389
Disease: Amyloidosis, familial visceral
15 0.807 0.200 12 69350192 missense variant T/C snv 0.800 1.000 1 1993 1993
Amyloidosis
CUI: C0002726
Disease: Amyloidosis
93 0.807 0.200 12 69350192 missense variant T/C snv 0.010 1.000 1 1999 1999
Amyloidosis, Familial
CUI: C0740340
Disease: Amyloidosis, Familial
12 0.807 0.200 12 69350192 missense variant T/C snv 0.010 1.000 1 2010 2010
Hereditary systemic amyloidosis
CUI: C4081731
Disease: Hereditary systemic amyloidosis
6 0.807 0.200 12 69350192 missense variant T/C snv 0.010 1.000 1 2004 2004
Petechiae
CUI: C0031256
Disease: Petechiae
5 0.807 0.200 12 69350192 missense variant T/C snv 0.010 1.000 1 1999 1999
Petechiae of skin
CUI: C0241144
Disease: Petechiae of skin
2 0.807 0.200 12 69350192 missense variant T/C snv 0.010 1.000 1 1999 1999
Plaque, Amyloid
CUI: C2936349
Disease: Plaque, Amyloid
10 0.807 0.200 12 69350192 missense variant T/C snv 0.010 1.000 1 2004 2004