rs63751165, MAPT

N. diseases: 3
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 0.925 0.120 17 46010401 missense variant G/A;T snv 0.830 1.000 3 1999 2005
Pick Disease of the Brain
CUI: C0236642
Disease: Pick Disease of the Brain
83 0.925 0.120 17 46010401 missense variant G/A;T snv 0.030 1.000 3 1999 2005
Parkinsonian Disorders
CUI: C0242422
Disease: Parkinsonian Disorders
95 0.925 0.120 17 46010401 missense variant G/A;T snv 0.020 1.000 2 2004 2005