rs200154785, APP

N. diseases: 2
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.
Henoch-Schoenlein Purpura
CUI: C0034152
Disease: Henoch-Schoenlein Purpura
59 0.925 0.240 21 25997362 missense variant T/A snv 0.010 1.000 1 2002 2002
Hereditary Autosomal Dominant Spastic Paraplegia
CUI: C0751602
Disease: Hereditary Autosomal Dominant Spastic Paraplegia
7 0.925 0.240 21 25997362 missense variant T/A snv 0.010 1.000 1 2002 2002