Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519913 0.925 0.120 1 11157172 missense variant G/C snv 3
rs786205165 0.882 0.120 1 11157173 missense variant C/A;T snv 4
rs1057519917 0.807 0.160 1 11124517 missense variant A/G;T snv 7
rs1057519914 0.851 0.240 1 11157174 missense variant A/G snv 5
rs587777894 0.776 0.240 1 11124516 missense variant G/A;T snv 9
rs530941076 0.695 0.280 17 7674873 missense variant A/C;G;T snv 4.0E-06 21
rs1057519929 0.776 0.320 3 179199066 missense variant G/A snv 10
rs1057519932 0.683 0.320 3 179234298 missense variant T/G snv 22
rs1057520003 0.695 0.320 17 7675996 missense variant T/G snv 20
rs121913274 0.645 0.320 3 179218304 missense variant A/C;G;T snv 33
rs121913275 0.672 0.320 3 179218305 missense variant G/A;C;T snv 4.0E-06 26
rs1057519983 0.724 0.360 17 7673797 missense variant A/G snv 16
rs1057520002 0.695 0.360 17 7674242 missense variant A/C;G snv 20
rs121912666 0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 34
rs587778720 0.667 0.360 17 7674893 missense variant C/A;G;T snv 4.0E-06 31
rs1057519992 0.742 0.400 17 7674890 missense variant T/A;C;G snv 14
rs121909229 0.683 0.400 10 87933148 missense variant G/A;C;T snv 23
rs121913255 0.667 0.400 1 114713907 missense variant T/A;G snv 26
rs786201057 0.677 0.400 17 7675995 missense variant G/A;C;T snv 24
rs104886003 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 71
rs1057520007 0.701 0.440 17 7674917 missense variant T/A;C;G snv 21
rs28934574 0.658 0.440 17 7673776 missense variant G/A;C snv 4.0E-06 31
rs397516436 0.641 0.440 17 7674894 stop gained G/A;C snv 34
rs730882008 0.683 0.440 17 7673775 missense variant C/A;G;T snv 4.0E-06 23
rs863224451 0.701 0.440 17 7673796 missense variant C/A;G;T snv 20