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.
Gilbert Disease (disorder)
CUI: C0017551
Disease: Gilbert Disease (disorder)
29 0.925 0.080 2 233760973 missense variant C/A;T snv 1.5E-03; 4.4E-05 0.730 1.000 3 2001 2007
Crigler Najjar syndrome, type 2
CUI: C2931132
Disease: Crigler Najjar syndrome, type 2
27 0.925 0.080 2 233760973 missense variant C/A;T snv 1.5E-03; 4.4E-05 0.710 1.000 1 2007 2007