rs63750424, MAPT

N. diseases: 30
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.
PARKINSON DISEASE, LATE-ONSET
CUI: C3160718
Disease: PARKINSON DISEASE, LATE-ONSET
76 0.677 0.240 17 46024061 missense variant C/T snv 1.6E-05 0.700 0
Supranuclear Palsy, Progressive, 1
CUI: C4551863
Disease: Supranuclear Palsy, Progressive, 1
6 0.677 0.240 17 46024061 missense variant C/T snv 1.6E-05 0.700 0
Supranuclear Palsy, Progressive, 1, Atypical
CUI: C1850077
Disease: Supranuclear Palsy, Progressive, 1, Atypical
4 0.677 0.240 17 46024061 missense variant C/T snv 1.6E-05 0.700 0
Progressive supranuclear palsy
CUI: C0038868
Disease: Progressive supranuclear palsy
52 0.677 0.240 17 46024061 missense variant C/T snv 1.6E-05 0.020 1.000 2 1999 2018
Corticobasal degeneration
CUI: C0393570
Disease: Corticobasal degeneration
14 0.677 0.240 17 46024061 missense variant C/T snv 1.6E-05 0.010 1.000 1 1999 1999
Mutism
CUI: C0026884
Disease: Mutism
4 0.677 0.240 17 46024061 missense variant C/T snv 1.6E-05 0.010 1.000 1 1999 1999
Frontotemporal dementia
CUI: C0338451
Disease: Frontotemporal dementia
215 0.677 0.240 17 46024061 missense variant C/T snv 1.6E-05 0.800 1.000 12 2000 2019
Pick Disease of the Brain
CUI: C0236642
Disease: Pick Disease of the Brain
83 0.677 0.240 17 46024061 missense variant C/T snv 1.6E-05 0.760 1.000 6 2000 2019
Senile Plaques
CUI: C0333463
Disease: Senile Plaques
21 0.677 0.240 17 46024061 missense variant C/T snv 1.6E-05 0.020 1.000 2 2000 2015
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.677 0.240 17 46024061 missense variant C/T snv 1.6E-05 0.080 1.000 8 2002 2019
Tauopathies
CUI: C0949664
Disease: Tauopathies
43 0.677 0.240 17 46024061 missense variant C/T snv 1.6E-05 0.070 1.000 7 2002 2018
Memory impairment
CUI: C0233794
Disease: Memory impairment
48 0.677 0.240 17 46024061 missense variant C/T snv 1.6E-05 0.020 1.000 2 2002 2018
Presenile dementia
CUI: C0011265
Disease: Presenile dementia
159 0.677 0.240 17 46024061 missense variant C/T snv 1.6E-05 0.040 1.000 4 2003 2014
Dementia
CUI: C0497327
Disease: Dementia
176 0.677 0.240 17 46024061 missense variant C/T snv 1.6E-05 0.030 1.000 3 2003 2014
Anxiety
CUI: C0003467
Disease: Anxiety
287 0.677 0.240 17 46024061 missense variant C/T snv 1.6E-05 0.010 1.000 1 2005 2005
Anxiety Disorders
CUI: C0003469
Disease: Anxiety Disorders
163 0.677 0.240 17 46024061 missense variant C/T snv 1.6E-05 0.010 1.000 1 2005 2005
Depressed mood
CUI: C0344315
Disease: Depressed mood
269 0.677 0.240 17 46024061 missense variant C/T snv 1.6E-05 0.010 1.000 1 2005 2005
Depressive disorder
CUI: C0011581
Disease: Depressive disorder
297 0.677 0.240 17 46024061 missense variant C/T snv 1.6E-05 0.010 1.000 1 2005 2005
Mental Depression
CUI: C0011570
Disease: Mental Depression
271 0.677 0.240 17 46024061 missense variant C/T snv 1.6E-05 0.010 1.000 1 2005 2005
Familial Alzheimer's disease of early onset
CUI: C0338445
Disease: Familial Alzheimer's disease of early onset
33 0.677 0.240 17 46024061 missense variant C/T snv 1.6E-05 0.010 1.000 1 2008 2008
Familial Dementia
CUI: C0751071
Disease: Familial Dementia
5 0.677 0.240 17 46024061 missense variant C/T snv 1.6E-05 0.010 1.000 1 2008 2008
Language Problems
CUI: C1405458
Disease: Language Problems
2 0.677 0.240 17 46024061 missense variant C/T snv 1.6E-05 0.010 1.000 1 2008 2008
Cognition Disorders
CUI: C0009241
Disease: Cognition Disorders
47 0.677 0.240 17 46024061 missense variant C/T snv 1.6E-05 0.010 1.000 1 2013 2013
Impaired cognition
CUI: C0338656
Disease: Impaired cognition
348 0.677 0.240 17 46024061 missense variant C/T snv 1.6E-05 0.010 1.000 1 2013 2013
Parkinsonian Disorders
CUI: C0242422
Disease: Parkinsonian Disorders
95 0.677 0.240 17 46024061 missense variant C/T snv 1.6E-05 0.030 1.000 3 2014 2018