rs1556300621, PRPS1

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.
Hearing Loss
CUI: C3887873
Disease: Hearing Loss
61 X 107645286 missense variant C/T snv 0.700 0
Retinal Dystrophies
CUI: C0854723
Disease: Retinal Dystrophies
227 X 107645286 missense variant C/T snv 0.700 0