rs762046989, MAPT

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.
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.851 0.200 17 45971867 missense variant C/G snv 8.0E-06 0.010 1.000 1 2019 2019
Frontotemporal dementia
CUI: C0338451
Disease: Frontotemporal dementia
215 0.851 0.200 17 45971867 missense variant C/G snv 8.0E-06 0.010 1.000 1 2016 2016
Language Disorders
CUI: C0023015
Disease: Language Disorders
25 0.851 0.200 17 45971867 missense variant C/G snv 8.0E-06 0.010 1.000 1 2019 2019
Primary Progressive Nonfluent Aphasia
CUI: C0751706
Disease: Primary Progressive Nonfluent Aphasia
13 0.851 0.200 17 45971867 missense variant C/G snv 8.0E-06 0.010 1.000 1 2016 2016
Progressive supranuclear palsy
CUI: C0038868
Disease: Progressive supranuclear palsy
52 0.851 0.200 17 45971867 missense variant C/G snv 8.0E-06 0.010 1.000 1 2016 2016