rs63750680, PSEN1

N. diseases: 2
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.
Parkinsonian Disorders
CUI: C0242422
Disease: Parkinsonian Disorders
95 1.000 0.080 14 73198076 missense variant T/C snv 0.010 1.000 1 2004 2004
Subcortical dementia
CUI: C4024935
Disease: Subcortical dementia
2 1.000 0.080 14 73198076 missense variant T/C snv 0.010 1.000 1 2004 2004