rs242557, MAPT

N. diseases: 12
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.
Progressive supranuclear palsy
CUI: C0038868
Disease: Progressive supranuclear palsy
52 0.752 0.200 17 45942346 intron variant G/A snv 0.36 0.860 1.000 8 2010 2019
Atrial Fibrillation
CUI: C0004238
Disease: Atrial Fibrillation
584 0.752 0.200 17 45942346 intron variant G/A snv 0.36 0.700 1.000 1 2018 2018
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.752 0.200 17 45942346 intron variant G/A snv 0.36 0.060 0.833 6 2008 2017
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
990 0.752 0.200 17 45942346 intron variant G/A snv 0.36 0.060 1.000 6 2010 2017
Deuteranomaly
CUI: C3887938
Disease: Deuteranomaly
10 0.752 0.200 17 45942346 intron variant G/A snv 0.36 0.030 1.000 3 2011 2017
Alzheimer Disease, Late Onset
CUI: C0494463
Disease: Alzheimer Disease, Late Onset
243 0.752 0.200 17 45942346 intron variant G/A snv 0.36 0.010 1 2007 2007
Corticobasal degeneration
CUI: C0393570
Disease: Corticobasal degeneration
14 0.752 0.200 17 45942346 intron variant G/A snv 0.36 0.010 1.000 1 2017 2017
Dementia
CUI: C0497327
Disease: Dementia
176 0.752 0.200 17 45942346 intron variant G/A snv 0.36 0.010 1.000 1 2019 2019
Parkinsonian Disorders
CUI: C0242422
Disease: Parkinsonian Disorders
95 0.752 0.200 17 45942346 intron variant G/A snv 0.36 0.010 1.000 1 2011 2011
PNEUMOTHORAX, PRIMARY SPONTANEOUS
CUI: C1868193
Disease: PNEUMOTHORAX, PRIMARY SPONTANEOUS
15 0.752 0.200 17 45942346 intron variant G/A snv 0.36 0.010 1.000 1 2010 2010
Presenile dementia
CUI: C0011265
Disease: Presenile dementia
159 0.752 0.200 17 45942346 intron variant G/A snv 0.36 0.010 1.000 1 2019 2019
Tauopathies
CUI: C0949664
Disease: Tauopathies
43 0.752 0.200 17 45942346 intron variant G/A snv 0.36 0.010 1.000 1 2019 2019