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: rs121908094
rs121908094
3 0.925 0.160 1 40258392 stop gained C/T snv 8.0E-06 0.010 1.000 1 2008 2008
dbSNP: rs121908095
rs121908095
3 0.925 0.160 1 40272009 missense variant C/G;T snv 2.0E-05 0.010 1.000 1 2008 2008
dbSNP: rs29001566
rs29001566
RHO
10 0.807 0.080 3 129533711 missense variant C/A;G;T snv 0.010 1.000 1 2015 2015
dbSNP: rs58850446
rs58850446
3 0.925 0.200 1 156134908 missense variant T/C snv 0.010 1.000 1 2008 2008