Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397516436 0.641 0.440 17 7674894 stop gained G/A;C snv 34
rs121913274 0.645 0.320 3 179218304 missense variant A/C;G;T snv 33
rs760043106 0.645 0.440 17 7674947 missense variant A/C;G;T snv 32
rs886039484 0.641 0.440 17 7674888 missense variant T/C;G snv 32
rs28934574 0.658 0.440 17 7673776 missense variant G/A;C snv 4.0E-06 31
rs587778720 0.667 0.360 17 7674893 missense variant C/A;G;T snv 4.0E-06 31
rs104894226 0.658 0.560 11 534285 missense variant C/A;G;T snv 29
rs121912656 0.662 0.560 17 7674229 missense variant C/A;G;T snv 4.0E-06; 4.0E-06 28
rs121913495 0.672 0.400 20 58909366 missense variant G/A;T snv 28
rs28934573 0.667 0.480 17 7674241 missense variant G/A;C;T snv 4.0E-06 28
rs28933406 0.667 0.480 11 533875 missense variant G/C;T snv 27
rs1057519991 0.662 0.440 17 7675076 missense variant T/A;C;G snv 4.0E-06 26
rs121912660 0.683 0.240 17 7673781 missense variant C/A;G;T snv 26
rs121913275 0.672 0.320 3 179218305 missense variant G/A;C;T snv 4.0E-06 26
rs1057519925 0.683 0.560 3 179210291 missense variant G/A;C snv 25
rs121909218 0.672 0.360 10 87933145 missense variant G/A snv 25
rs138729528 0.677 0.480 17 7675089 missense variant G/A;C snv 1.6E-05 25
rs6505162 0.695 0.320 17 30117165 5 prime UTR variant A/C;T snv 0.50; 3.1E-05 25
rs764146326 0.662 0.480 17 7673779 missense variant C/A;G;T snv 4.0E-06 25
rs121912657 0.683 0.480 17 7673806 missense variant C/A;G;T snv 4.0E-06 24
rs587780070 0.683 0.320 17 7675077 missense variant G/A;C;T snv 4.0E-06 24
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 24
rs876658468 0.689 0.440 17 7674954 missense variant G/A;C;T snv 24
rs1057519747 0.716 0.280 17 7675094 missense variant A/C;G;T snv 23