rs63751011, MAPT

N. diseases: 4
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 46010418 intron variant C/T snv 0.700 1.000 11 1998 2016
Dementia
CUI: C0497327
Disease: Dementia
176 0.925 0.120 17 46010418 intron variant C/T snv 0.700 0
Memory impairment
CUI: C0233794
Disease: Memory impairment
48 0.925 0.120 17 46010418 intron variant C/T snv 0.700 0
Mental deterioration
CUI: C0234985
Disease: Mental deterioration
121 0.925 0.120 17 46010418 intron variant C/T snv 0.700 0