rs61755800, PRPH2

N. diseases: 1
Source: CLINVAR ×
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.
Retinitis Pigmentosa
CUI: C0035334
Disease: Retinitis Pigmentosa
420 0.882 0.080 6 42704559 missense variant T/C;G snv 8.0E-06 0.710 1.000 1 1993 2008