rs10812774, LINGO2

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.
Essential Tremor
CUI: C0270736
Disease: Essential Tremor
79 0.925 0.040 9 28294233 intron variant T/C snv 0.49 0.010 1.000 1 2011 2011
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
990 0.925 0.040 9 28294233 intron variant T/C snv 0.49 0.010 1.000 1 2011 2011