Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519975 0.649 0.480 17 7675209 missense variant A/C;G;T snv 34
rs121912666 0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 34
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
rs7679673 0.677 0.440 4 105140377 intron variant C/A snv 0.50 28
rs17851045 0.672 0.400 12 25227341 missense variant T/A;G snv 4.0E-06 27
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
rs138729528 0.677 0.480 17 7675089 missense variant G/A;C snv 1.6E-05 25
rs764146326 0.662 0.480 17 7673779 missense variant C/A;G;T snv 4.0E-06 25
rs876658657 0.677 0.280 3 37020356 missense variant A/G snv 4.0E-06 25
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
rs587782329 0.677 0.280 17 7674217 missense variant C/A;G;T snv 23