rs386134131, CP

N. diseases: 1
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.
Ceruloplasmin deficiency
CUI: C0878682
Disease: Ceruloplasmin deficiency
51 1.000 0.080 3 149178618 missense variant C/T snv 0.700 0