rs63750959, 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.
Supranuclear Palsy, Progressive, 1
CUI: C4551863
Disease: Supranuclear Palsy, Progressive, 1
6 0.827 0.200 17 45962351 missense variant G/A;T snv 6.0E-05 0.800 0
Frontotemporal dementia
CUI: C0338451
Disease: Frontotemporal dementia
215 0.827 0.200 17 45962351 missense variant G/A;T snv 6.0E-05 0.710 1.000 2 2002 2010
Dementia
CUI: C0497327
Disease: Dementia
176 0.827 0.200 17 45962351 missense variant G/A;T snv 6.0E-05 0.010 1.000 1 2002 2002
Pick Disease of the Brain
CUI: C0236642
Disease: Pick Disease of the Brain
83 0.827 0.200 17 45962351 missense variant G/A;T snv 6.0E-05 0.010 1.000 1 2002 2002
Presenile dementia
CUI: C0011265
Disease: Presenile dementia
159 0.827 0.200 17 45962351 missense variant G/A;T snv 6.0E-05 0.010 1.000 1 2002 2002