rs9468, MAPT

N. diseases: 6
Disease: Parkinson Disease ×
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.
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
990 0.882 0.080 17 46024197 3 prime UTR variant T/C snv 0.15 0.14 0.030 1.000 3 2012 2019