rs1216578110, 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.
Impaired cognition
CUI: C0338656
Disease: Impaired cognition
348 1.000 0.040 21 25955652 missense variant T/C snv 4.0E-06 7.0E-06 0.010 1.000 1 2018 2018