rs63749855, MAPT

N. diseases: 8
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 0.790 0.200 17 46014271 missense variant T/G snv 0.010 1.000 1 2019 2019
Dementia
CUI: C0497327
Disease: Dementia
176 0.790 0.200 17 46014271 missense variant T/G snv 0.010 1.000 1 2003 2003
Familial (FPAH)
CUI: C1611743
Disease: Familial (FPAH)
276 0.790 0.200 17 46014271 missense variant T/G snv 0.010 1.000 1 2003 2003
Frontotemporal dementia
CUI: C0338451
Disease: Frontotemporal dementia
215 0.790 0.200 17 46014271 missense variant T/G snv 0.010 1.000 1 2003 2003
Language Disorders
CUI: C0023015
Disease: Language Disorders
25 0.790 0.200 17 46014271 missense variant T/G snv 0.010 1.000 1 2019 2019
Pick Disease of the Brain
CUI: C0236642
Disease: Pick Disease of the Brain
83 0.790 0.200 17 46014271 missense variant T/G snv 0.010 1.000 1 2003 2003
Presenile dementia
CUI: C0011265
Disease: Presenile dementia
159 0.790 0.200 17 46014271 missense variant T/G snv 0.010 1.000 1 2003 2003
Progressive supranuclear palsy
CUI: C0038868
Disease: Progressive supranuclear palsy
52 0.790 0.200 17 46014271 missense variant T/G snv 0.010 1.000 1 2011 2011