rs74315401, PRNP

N. diseases: 32
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.
Myopathy
CUI: C0026848
Disease: Myopathy
166 0.683 0.320 20 4699525 missense variant C/T snv 0.010 1.000 1 1996 1996