Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1064795104 0.790 0.440 2 72498492 stop gained A/C snv 17
rs1561273261 0.790 0.160 5 62361307 missense variant G/A snv 17
rs28940881 0.776 0.200 11 89177954 start lost A/G snv 6.4E-05 5.6E-05 16
rs758361736 0.776 0.240 15 89649836 missense variant T/G snv 1.3E-05 1.4E-05 16
rs121908212 0.732 0.160 19 13303877 missense variant G/A snv 14
rs869312824 0.827 0.200 1 1804565 missense variant A/G snv 14
rs137852834 0.763 0.280 12 88083936 stop gained T/A snv 5.5E-05 9.1E-05 13
rs748787734 0.827 0.240 19 6495437 missense variant G/A;C snv 1.2E-05 13
rs121907922 0.742 0.320 11 31789935 stop gained T/A snv 12
rs1135402761 0.827 0.320 12 79448958 missense variant T/C snv 11
rs142285818
RHO
0.807 0.120 3 129532727 missense variant C/G;T snv 9.7E-04 4.1E-04 11
rs150726175 0.776 0.200 1 9982630 missense variant G/A snv 7.0E-04 8.5E-04 11
rs886039807 0.776 0.480 16 75541466 non coding transcript exon variant A/G snv 4.2E-06 11
rs138504221 0.807 0.280 17 80212128 missense variant A/G snv 9.6E-05 1.5E-04 9
rs144078282 0.776 0.400 11 72302339 missense variant T/A;C snv 1.8E-04; 2.0E-04 9
rs200203460 0.776 0.400 11 72302312 stop gained G/A;C;T snv 2.8E-05 9
rs778361520 0.925 0.120 1 31728621 missense variant G/A snv 8.0E-06 2.1E-05 9
rs61754381 0.790 0.200 11 89227816 splice region variant T/A;C snv 9.5E-04; 8.0E-06 8
rs770703007 0.851 0.120 16 1706450 stop gained C/G;T snv 4.0E-06 8
rs864309532 0.807 0.360 X 134393952 missense variant G/A snv 7
rs1057518963 0.851 0.200 X 68210239 missense variant A/G snv 6
rs1114167292 0.882 0.080 3 197704686 missense variant C/T snv 1.4E-05 6
rs1488635637 0.827 0.360 17 58208003 splice acceptor variant T/C;G snv 7.0E-06 6
rs28940893 0.827 0.160 22 50625392 missense variant G/A snv 3.9E-04 3.6E-04 6
rs757788894 0.882 0.120 16 1449081 missense variant C/T snv 4.0E-06 6