rs786205579, PRPH2

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.
Low Vision
CUI: C0042798
Disease: Low Vision
51 0.925 0.120 6 42721838 missense variant C/T snv 0.010 1.000 1 2016 2016
Nystagmus
CUI: C0028738
Disease: Nystagmus
95 0.925 0.120 6 42721838 missense variant C/T snv 0.010 1.000 1 2016 2016