rs3794087, SLC1A2

N. diseases: 6
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 0.120 11 35308068 intron variant G/T snv 0.20 0.900 0.500 10 2012 2018
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
990 0.851 0.120 11 35308068 intron variant G/T snv 0.20 0.020 0.500 2 2016 2018
Amyotrophic Lateral Sclerosis
CUI: C0002736
Disease: Amyotrophic Lateral Sclerosis
485 0.851 0.120 11 35308068 intron variant G/T snv 0.20 0.010 1.000 1 2016 2016
Migraine Disorders
CUI: C0149931
Disease: Migraine Disorders
264 0.851 0.120 11 35308068 intron variant G/T snv 0.20 0.010 1 2014 2014
Restless Legs Syndrome
CUI: C0035258
Disease: Restless Legs Syndrome
72 0.851 0.120 11 35308068 intron variant G/T snv 0.20 0.010 1 2014 2014
Tremor
CUI: C0040822
Disease: Tremor
52 0.851 0.120 11 35308068 intron variant G/T snv 0.20 0.010 1.000 1 2013 2013