rs201817335, APP

N. diseases: 1
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.
Myoclonus
CUI: C0027066
Disease: Myoclonus
34 21 26051139 missense variant C/T snv 4.0E-06 0.010 1.000 1 2015 2015