Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121909646 0.882 0.120 13 28018504 missense variant T/A;G snv 1
rs121912472 0.925 0.080 9 5073742 missense variant G/C snv 1
rs121913232 0.925 0.120 13 28018500 missense variant G/C snv 1
rs121913233 0.627 0.520 11 533874 missense variant T/A;C;G snv 1
rs121913240 0.672 0.440 12 25227342 missense variant T/A;C;G snv 1
rs121913250 0.683 0.440 1 114716127 missense variant C/A;G;T snv 1
rs121913488 0.807 0.120 13 28018505 missense variant C/A;G;T snv 1
rs121913503 0.689 0.200 15 90088606 missense variant C/A;T snv 1
rs121913514
KIT
0.763 0.240 4 54733174 missense variant T/A;G snv 1
rs121917759 0.790 0.480 11 533466 missense variant G/A snv 1
rs121918464 0.708 0.440 12 112450406 missense variant G/A;C snv 1
rs137854451 0.925 0.080 19 856000 missense variant G/A snv 1
rs267606870 0.763 0.280 15 90088703 missense variant G/A;C snv 1
rs28931590 1.000 0.040 19 33302164 missense variant T/A snv 1
rs28933406 0.667 0.480 11 533875 missense variant G/C;T snv 1
rs387906629 0.925 0.080 3 128481270 missense variant G/A snv 1
rs483352695 0.882 0.200 17 7674227 missense variant T/A;C;G snv 1
rs57246956 0.882 0.080 19 855649 missense variant G/A;T snv 1
rs587781288 0.732 0.440 17 7675190 missense variant C/A;T snv 1
rs587782529 0.851 0.200 17 7670700 missense variant G/A;C snv 1
rs74315450 0.851 0.120 21 34859485 missense variant C/T snv 1
rs786201838 0.683 0.440 17 7674953 missense variant T/A;C;G snv 1
rs869312828 0.807 0.080 5 177512369 missense variant C/T snv 1