Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104894229 0.564 0.600 11 534289 missense variant C/A;G;T snv 52
rs11540652 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 42
rs28934576 0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 39
rs121912651 0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 37
rs104894230 0.564 0.600 11 534288 missense variant C/A;G;T snv 36
rs104894228 0.605 0.560 11 534286 missense variant C/A;G;T snv 30
rs121913343 0.611 0.520 17 7673803 missense variant G/A;C;T snv 1.2E-05 29
rs11554290 0.583 0.600 1 114713908 missense variant T/A;C;G snv 25
rs104894226 0.658 0.560 11 534285 missense variant C/A;G;T snv 23
rs28934874 0.695 0.480 17 7675161 missense variant G/A;C;T snv 21
rs1057519981 0.689 0.440 17 7674251 missense variant A/C;G;T snv 20
rs121913233 0.627 0.520 11 533874 missense variant T/A;C;G snv 20
rs587781525 0.689 0.480 17 7673778 missense variant T/A;C;G snv 20
rs730882005 0.701 0.400 17 7674250 missense variant C/A;G;T snv 8.0E-06 20
rs764146326 0.662 0.480 17 7673779 missense variant C/A;G;T snv 4.0E-06 20
rs121913255 0.667 0.400 1 114713907 missense variant T/A;G snv 19
rs1057520007 0.701 0.440 17 7674917 missense variant T/A;C;G snv 17
rs28933406 0.667 0.480 11 533875 missense variant G/C;T snv 17
rs121912657 0.683 0.480 17 7673806 missense variant C/A;G;T snv 4.0E-06 15
rs17851045 0.672 0.400 12 25227341 missense variant T/A;G snv 4.0E-06 15
rs587781288 0.732 0.440 17 7675190 missense variant C/A;T snv 15
rs876659802 0.732 0.440 17 7673787 missense variant G/A;C;T snv 15
rs17849781 0.701 0.480 17 7673788 missense variant G/A;C;T snv 14
rs1057519977 0.763 0.360 17 7675189 missense variant G/C snv 13
rs876660333 0.742 0.360 17 7673805 missense variant A/C;G;T snv 13