rs63750635, 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.
Pick Disease of the Brain
CUI: C0236642
Disease: Pick Disease of the Brain
83 0.851 0.120 17 46014286 missense variant C/T snv 0.810 1.000 5 1999 2002
Frontotemporal dementia
CUI: C0338451
Disease: Frontotemporal dementia
215 0.851 0.120 17 46014286 missense variant C/T snv 0.700 0
Presenile dementia
CUI: C0011265
Disease: Presenile dementia
159 0.851 0.120 17 46014286 missense variant C/T snv 0.020 1.000 2 2002 2003
Dementia
CUI: C0497327
Disease: Dementia
176 0.851 0.120 17 46014286 missense variant C/T snv 0.010 1.000 1 2003 2003
Tauopathies
CUI: C0949664
Disease: Tauopathies
43 0.851 0.120 17 46014286 missense variant C/T snv 0.010 1.000 1 2002 2002