rs11856808, LINGO1

N. diseases: 5
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 0.827 0.120 15 77680428 intron variant C/T snv 0.42 0.030 0.667 3 2010 2012
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
990 0.827 0.120 15 77680428 intron variant C/T snv 0.42 0.030 0.667 3 2010 2015
Familial (FPAH)
CUI: C1611743
Disease: Familial (FPAH)
276 0.827 0.120 15 77680428 intron variant C/T snv 0.42 0.010 1.000 1 2012 2012
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
1022 0.827 0.120 15 77680428 intron variant C/T snv 0.42 0.010 1 2013 2013
Symphysis Pubis Dysfunction
CUI: C2609259
Disease: Symphysis Pubis Dysfunction
4 0.827 0.120 15 77680428 intron variant C/T snv 0.42 0.010 1 2010 2010