rs267606980, 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 0.080 20 4699600 missense variant G/T snv 4.0E-06 0.030 1.000 3 2017 2020
Acquired prion disease
CUI: C4303462
Disease: Acquired prion disease
1 1.000 0.080 20 4699600 missense variant G/T snv 4.0E-06 0.010 1.000 1 2015 2015