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.
HHH syndrome
CUI: C0268540
Disease: HHH syndrome
21 1.000 0.160 13 40799080 missense variant G/A snv 2.0E-05 0.800 1.000 7 1999 2009