Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs29001566
rs29001566
RHO
10 0.807 0.080 3 129533711 missense variant C/A;G;T snv 0.700 0
dbSNP: rs61755787
rs61755787
PRPH2
5 0.882 0.120 6 42721866 missense variant C/T snv 0.700 0