rs778250646, 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.
Channelopathies
CUI: C1720983
Disease: Channelopathies
8 0.925 0.080 21 26112008 missense variant T/C snv 4.0E-06 0.010 1 2010 2010
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
990 0.925 0.080 21 26112008 missense variant T/C snv 4.0E-06 0.010 1.000 1 2010 2010