rs552184470, GUCY2D

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.
Electroretinogram abnormal
CUI: C0476397
Disease: Electroretinogram abnormal
10 1.000 0.080 17 8003171 inframe deletion TCTGCT/- delins 1.8E-03 1.9E-03 0.700 0
Nystagmus
CUI: C0028738
Disease: Nystagmus
95 1.000 0.080 17 8003171 inframe deletion TCTGCT/- delins 1.8E-03 1.9E-03 0.700 0