rs63750570, 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.
Frontotemporal dementia
CUI: C0338451
Disease: Frontotemporal dementia
215 0.827 0.120 17 46018629 missense variant G/A snv 0.850 1.000 26 1998 2017
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.827 0.120 17 46018629 missense variant G/A snv 0.040 1.000 4 1998 2017
Dementia
CUI: C0497327
Disease: Dementia
176 0.827 0.120 17 46018629 missense variant G/A snv 0.010 1.000 1 2001 2001
Familial (FPAH)
CUI: C1611743
Disease: Familial (FPAH)
276 0.827 0.120 17 46018629 missense variant G/A snv 0.010 1.000 1 2005 2005
Impulsive Behavior
CUI: C0021125
Disease: Impulsive Behavior
69 0.827 0.120 17 46018629 missense variant G/A snv 0.010 1.000 1 2007 2007
Neurodegenerative Disorders
CUI: C0524851
Disease: Neurodegenerative Disorders
85 0.827 0.120 17 46018629 missense variant G/A snv 0.010 1.000 1 2016 2016
Pick Disease of the Brain
CUI: C0236642
Disease: Pick Disease of the Brain
83 0.827 0.120 17 46018629 missense variant G/A snv 0.010 1.000 1 2017 2017
Tauopathies
CUI: C0949664
Disease: Tauopathies
43 0.827 0.120 17 46018629 missense variant G/A snv 0.010 1.000 1 2001 2001