rs63750869, MAPT

N. diseases: 6
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.
Primary Progressive Nonfluent Aphasia
CUI: C0751706
Disease: Primary Progressive Nonfluent Aphasia
13 0.827 0.160 17 46018707 missense variant G/A snv 2.4E-05 5.6E-05 0.020 1.000 2 2007 2011
Frontotemporal dementia
CUI: C0338451
Disease: Frontotemporal dementia
215 0.827 0.160 17 46018707 missense variant G/A snv 2.4E-05 5.6E-05 0.010 1.000 1 2011 2011
Neurodegenerative Disorders
CUI: C0524851
Disease: Neurodegenerative Disorders
85 0.827 0.160 17 46018707 missense variant G/A snv 2.4E-05 5.6E-05 0.010 1.000 1 2011 2011
Pick Disease of the Brain
CUI: C0236642
Disease: Pick Disease of the Brain
83 0.827 0.160 17 46018707 missense variant G/A snv 2.4E-05 5.6E-05 0.010 1.000 1 2011 2011
Posterior cortical atrophy syndrome
CUI: C4275079
Disease: Posterior cortical atrophy syndrome
8 0.827 0.160 17 46018707 missense variant G/A snv 2.4E-05 5.6E-05 0.010 1.000 1 2014 2014
Semantic Dementia
CUI: C0338462
Disease: Semantic Dementia
4 0.827 0.160 17 46018707 missense variant G/A snv 2.4E-05 5.6E-05 0.010 1.000 1 2010 2010