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.
Blindness
CUI: C0456909
Disease: Blindness
34 MT 14598 missense variant T/C snv 0.700 0
Parkinsonian Disorders
CUI: C0242422
Disease: Parkinsonian Disorders
95 MT 14598 missense variant T/C snv 0.700 0