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.
Fabry Disease
CUI: C0002986
Disease: Fabry Disease
206 0.925 0.200 X 101397871 missense variant T/C snv 0.810 1.000 31 1989 2017
Neuralgia
CUI: C0027796
Disease: Neuralgia
16 0.925 0.200 X 101397871 missense variant T/C snv 0.010 1.000 1 2003 2003
Ventricular hypertrophy
CUI: C0340279
Disease: Ventricular hypertrophy
9 0.925 0.200 X 101397871 missense variant T/C snv 0.010 1.000 1 2003 2003