rs372878791, PRNP

N. diseases: 2
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.
Prion Diseases
CUI: C0162534
Disease: Prion Diseases
67 1.000 0.120 20 4699783 missense variant C/G;T snv 3.2E-05; 4.0E-05 0.020 1.000 2 2002 2010
Creutzfeldt-Jakob Disease, Familial
CUI: C0751254
Disease: Creutzfeldt-Jakob Disease, Familial
16 1.000 0.120 20 4699783 missense variant C/G;T snv 3.2E-05; 4.0E-05 0.010 1.000 1 2010 2010