Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs72547551 0.882 0.160 16 89550545 missense variant C/T snv 3.6E-05 1.5E-04 5
rs748309520 0.882 0.160 16 89531903 splice acceptor variant G/A snv 1.6E-05 7.0E-06 5
rs752989523 0.882 0.160 16 89553853 stop gained G/A;C snv 8.0E-06 5
rs879253797 0.882 0.160 16 89556954 missense variant C/T snv 1.4E-05 5
rs765468645 0.882 0.160 8 93765413 stop gained C/T snv 8.0E-06 2.1E-05 5
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
rs1488635637 0.827 0.360 17 58208003 splice acceptor variant T/C;G snv 7.0E-06 6
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
rs767982852 0.882 0.080 3 197694417 missense variant T/C snv 8.0E-06 4.9E-05 6
rs730882209 0.925 0.080 9 132326375 frameshift variant -/C delins 6
rs1553281318 0.882 0.120 1 226986536 frameshift variant -/A delins 7
rs864309532 0.807 0.360 X 134393952 missense variant G/A snv 7
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
rs752914124 0.827 0.280 17 80210679 stop gained GGAGGTCCTTG/- del 8
rs778361520 0.925 0.120 1 31728621 missense variant G/A snv 8.0E-06 2.1E-05 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
rs1555350397 0.827 0.200 14 56804268 frameshift variant ACA/CC delins 9
rs138504221 0.807 0.280 17 80212128 missense variant A/G snv 9.6E-05 1.5E-04 9
rs886039809 0.807 0.480 14 58498824 frameshift variant A/- del 11
rs150726175 0.776 0.200 1 9982630 missense variant G/A snv 7.0E-04 8.5E-04 11
rs142285818
RHO
0.807 0.120 3 129532727 missense variant C/G;T snv 9.7E-04 4.1E-04 11