rs753737986, 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.
Hereditary Cerebral Amyloid Angiopathy, Icelandic Type
2 0.925 0.200 21 26111983 missense variant T/A snv 4.0E-06 0.010 1 2007 2007
Plaque, Amyloid
CUI: C2936349
Disease: Plaque, Amyloid
10 0.925 0.200 21 26111983 missense variant T/A snv 4.0E-06 0.010 1.000 1 2004 2004