Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104893768
RHO
0.807 0.080 3 129528801 missense variant C/A snv 8
rs113624356 0.724 0.400 11 66526181 missense variant T/G snv 1.5E-03 2.1E-03 7
rs80338902 0.790 0.200 1 216247118 missense variant C/A snv 9.7E-04 1.3E-03 7
rs104893775
RHO
0.807 0.160 3 129530917 missense variant C/T snv 6
rs29001566
RHO
0.807 0.080 3 129533711 missense variant C/A;G;T snv 6
rs61751374 0.776 0.160 1 94043413 missense variant G/A snv 1.7E-03 1.7E-03 5
rs121912550 0.827 0.120 7 128398557 missense variant C/T snv 4.0E-06 5
rs28937873 0.807 0.160 15 71813573 missense variant G/A snv 4.0E-04 3.1E-04 5
rs104893769
RHO
0.807 0.160 3 129528783 missense variant C/T snv 7.0E-06 5
rs201471607 0.851 0.080 1 94046943 missense variant T/C snv 1.4E-04 7.7E-05 4
rs111033258 0.851 0.200 3 150972565 missense variant A/C snv 2.7E-04 1.5E-04 4
rs111033267 0.851 0.200 3 150972520 stop gained G/A;T snv 1.2E-05; 1.2E-05 4
rs61748436
CRX
0.851 0.080 19 47836264 missense variant G/A snv 1.4E-05 4
rs763544450
ERG
1.000 0.080 21 38445560 missense variant T/G snv 4.0E-06 4
rs1177783734 0.925 0.080 8 18083991 missense variant T/G snv 4.5E-06 7.0E-06 4
rs111033260 0.790 0.200 10 54317414 stop gained G/A;T snv 2.2E-04; 4.0E-06 4
rs61755798 0.827 0.080 6 42704564 missense variant G/A;C snv 4
rs62645944 0.807 0.080 1 94098794 splice region variant C/A snv 8.8E-05 6.3E-05 3
rs104894559
CA4
0.882 0.200 17 60150074 missense variant C/T snv 2.5E-04 1.4E-04 3
rs912923677 0.851 0.240 20 10407704 missense variant T/C snv 4.0E-06 3
rs121912631 0.851 0.080 15 71811530 missense variant G/A;T snv 3
rs104894459
NRL
0.882 0.080 14 24082701 missense variant A/T snv 3
rs119475042 0.882 0.080 19 54123867 missense variant G/A;C snv 4.0E-06 3
rs61755771 0.827 0.160 6 42722199 stop gained G/A snv 1.6E-05 1.4E-05 3
rs61755793 0.807 0.080 6 42721820 missense variant C/T snv 4.0E-06 3