rs63750416, MAPT

N. diseases: 7
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.
Frontotemporal dementia
CUI: C0338451
Disease: Frontotemporal dementia
215 0.851 0.120 17 46010373 missense variant A/C snv 0.720 1.000 21 1998 2017
Pick Disease of the Brain
CUI: C0236642
Disease: Pick Disease of the Brain
83 0.851 0.120 17 46010373 missense variant A/C snv 0.020 1.000 2 2001 2017
Dementia in Parkinson's disease
CUI: C0349081
Disease: Dementia in Parkinson's disease
2 0.851 0.120 17 46010373 missense variant A/C snv 0.010 1.000 1 2002 2002
Familial (FPAH)
CUI: C1611743
Disease: Familial (FPAH)
276 0.851 0.120 17 46010373 missense variant A/C snv 0.010 1.000 1 2001 2001
Hyperactive behavior
CUI: C0424295
Disease: Hyperactive behavior
112 0.851 0.120 17 46010373 missense variant A/C snv 0.010 1.000 1 2017 2017
Parkinsonian Disorders
CUI: C0242422
Disease: Parkinsonian Disorders
95 0.851 0.120 17 46010373 missense variant A/C snv 0.010 1.000 1 2001 2001
Tauopathies
CUI: C0949664
Disease: Tauopathies
43 0.851 0.120 17 46010373 missense variant A/C snv 0.010 1.000 1 2017 2017