Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs28934576 0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 39
rs138729528 0.677 0.480 17 7675089 missense variant G/A;C snv 1.6E-05 25
rs753660142 0.708 0.280 17 7673782 missense variant T/C;G snv 1.6E-05 19
rs121913343 0.611 0.520 17 7673803 missense variant G/A;C;T snv 1.2E-05 29
rs11540652 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 42
rs121912666 0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 24
rs730882005 0.701 0.400 17 7674250 missense variant C/A;G;T snv 8.0E-06 20
rs747342068 0.695 0.440 17 7675218 missense variant T/C;G snv 4.0E-06 17
rs121912657 0.683 0.480 17 7673806 missense variant C/A;G;T snv 4.0E-06 15
rs786202962 0.701 0.320 17 7675085 missense variant C/A;T snv 4.0E-06 17
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
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
rs121912651 0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 37
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
rs397516436 0.641 0.440 17 7674894 stop gained G/A;C snv 26
rs28934575 0.641 0.400 17 7674230 missense variant C/A;G;T snv 25
rs786201057 0.677 0.400 17 7675995 missense variant G/A;C;T snv 24
rs786201838 0.683 0.440 17 7674953 missense variant T/A;C;G snv 23