Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs80357783 0.851 0.200 17 43124030 frameshift variant -/T delins 4.0E-06 6
rs397508983 1.000 17 43092959 stop gained G/A;C snv 4.0E-06 2
rs771203198 0.925 0.200 13 32394750 stop gained G/A;C snv 4.0E-06 3
rs121913500 0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 18
rs786202962 0.701 0.320 17 7675085 missense variant C/A;T snv 4.0E-06 17
rs80357310 0.925 0.200 17 43091870 stop gained C/A;G snv 4.0E-06 4
rs587780070 0.683 0.320 17 7675077 missense variant G/A;C;T snv 4.0E-06 23
rs1057519991 0.662 0.440 17 7675076 missense variant T/A;C;G snv 4.0E-06 19
rs530941076 0.695 0.280 17 7674873 missense variant A/C;G;T snv 4.0E-06 20
rs28934574 0.658 0.440 17 7673776 missense variant G/A;C snv 4.0E-06 27
rs80357303 0.925 0.200 17 43071113 stop gained T/A;G snv 4.0E-06 4
rs1057519738 0.790 0.160 17 39725079 missense variant G/A snv 4.0E-06 7
rs764146326 0.662 0.480 17 7673779 missense variant C/A;G;T snv 4.0E-06 20
rs730882008 0.683 0.440 17 7673775 missense variant C/A;G;T snv 4.0E-06 22
rs587778720 0.667 0.360 17 7674893 missense variant C/A;G;T snv 4.0E-06 25
rs121912656 0.662 0.560 17 7674229 missense variant C/A;G;T snv 4.0E-06; 4.0E-06 20
rs11554273 0.689 0.240 20 58909365 missense variant C/A;G;T snv 4.0E-06 17
rs121912651 0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 37
rs28934573 0.667 0.480 17 7674241 missense variant G/A;C;T snv 4.0E-06 24
rs483352697 0.695 0.480 17 7674944 missense variant C/A;G;T snv 4.0E-06 17
rs587782664 0.742 0.320 17 7674252 missense variant C/A;G;T snv 4.0E-06 14
rs80356962 0.807 0.200 17 43047666 stop gained C/G;T snv 4.0E-06 7.0E-06 8
rs1057519891 0.851 0.160 12 56088557 missense variant G/A;T snv 4.0E-06 5
rs104894229 0.564 0.600 11 534289 missense variant C/A;G;T snv 52
rs121913281 0.623 0.520 3 179234296 missense variant C/T snv 37