rs61752896, RPE65

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.
LEBER CONGENITAL AMAUROSIS, TYPE II (disorder)
CUI: C1859844
Disease: LEBER CONGENITAL AMAUROSIS, TYPE II (disorder)
36 0.925 0.080 1 68439571 missense variant A/C;G snv 4.0E-06; 8.0E-06 0.800 1.000 14 1997 2017
Retinitis Pigmentosa 20
CUI: C3151086
Disease: Retinitis Pigmentosa 20
27 0.925 0.080 1 68439571 missense variant A/C;G snv 4.0E-06; 8.0E-06 0.700 1.000 6 1998 2013