rs9652490, LINGO1

N. diseases: 4
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 0.851 0.080 15 77671545 intron variant A/G snv 0.28 0.900 0.714 14 2009 2016
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
990 0.851 0.080 15 77671545 intron variant A/G snv 0.28 0.080 0.625 8 2010 2015
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
1022 0.851 0.080 15 77671545 intron variant A/G snv 0.28 0.010 1 2013 2013
Sporadic Parkinson disease
CUI: C4511452
Disease: Sporadic Parkinson disease
65 0.851 0.080 15 77671545 intron variant A/G snv 0.28 0.010 1.000 1 2010 2010