rs1990622, None

N. diseases: 16
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.
Prion Diseases
CUI: C0162534
Disease: Prion Diseases
67 0.742 0.200 7 12244161 downstream gene variant A/G snv 0.52 0.700 1.000 1 2012 2012
Hippocampal sclerosis
CUI: C1504404
Disease: Hippocampal sclerosis
14 0.742 0.200 7 12244161 downstream gene variant A/G snv 0.52 0.010 1.000 1 2014 2014
Motor Neuron Disease
CUI: C0085084
Disease: Motor Neuron Disease
52 0.742 0.200 7 12244161 downstream gene variant A/G snv 0.52 0.010 1.000 1 2014 2014
Neurodegenerative Disorders
CUI: C0524851
Disease: Neurodegenerative Disorders
85 0.742 0.200 7 12244161 downstream gene variant A/G snv 0.52 0.010 1.000 1 2014 2014
Wernicke Encephalopathy
CUI: C0043121
Disease: Wernicke Encephalopathy
1 0.742 0.200 7 12244161 downstream gene variant A/G snv 0.52 0.010 1.000 1 2014 2014
Frontotemporal Lobar Degeneration
CUI: C0751072
Disease: Frontotemporal Lobar Degeneration
54 0.742 0.200 7 12244161 downstream gene variant A/G snv 0.52 0.040 1.000 4 2011 2015
GRN-related frontotemporal dementia
CUI: C3811918
Disease: GRN-related frontotemporal dementia
20 0.742 0.200 7 12244161 downstream gene variant A/G snv 0.52 0.030 1.000 3 2014 2015
Pick Disease of the Brain
CUI: C0236642
Disease: Pick Disease of the Brain
83 0.742 0.200 7 12244161 downstream gene variant A/G snv 0.52 0.010 1.000 1 2015 2015
Brain atrophy
CUI: C4551584
Disease: Brain atrophy
46 0.742 0.200 7 12244161 downstream gene variant A/G snv 0.52 0.010 1 2016 2016
Cerebral atrophy
CUI: C0235946
Disease: Cerebral atrophy
44 0.742 0.200 7 12244161 downstream gene variant A/G snv 0.52 0.010 1 2016 2016
Frontotemporal dementia
CUI: C0338451
Disease: Frontotemporal dementia
215 0.742 0.200 7 12244161 downstream gene variant A/G snv 0.52 0.040 1.000 4 2010 2017
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.742 0.200 7 12244161 downstream gene variant A/G snv 0.52 0.030 1.000 3 2011 2017
Bradykinesia
CUI: C0233565
Disease: Bradykinesia
16 0.742 0.200 7 12244161 downstream gene variant A/G snv 0.52 0.010 1.000 1 2017 2017
Muscle Rigidity
CUI: C0026837
Disease: Muscle Rigidity
25 0.742 0.200 7 12244161 downstream gene variant A/G snv 0.52 0.010 1.000 1 2017 2017
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
990 0.742 0.200 7 12244161 downstream gene variant A/G snv 0.52 0.010 1.000 1 2017 2017
Tremor
CUI: C0040822
Disease: Tremor
52 0.742 0.200 7 12244161 downstream gene variant A/G snv 0.52 0.010 1.000 1 2017 2017