rs2435207, MAPT

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.
Motor symptoms
CUI: C0426980
Disease: Motor symptoms
15 1.000 0.040 17 45981562 intron variant G/A snv 0.30 0.010 1.000 1 2012 2012
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
990 1.000 0.040 17 45981562 intron variant G/A snv 0.30 0.010 1 2009 2009