Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057520003 0.685 0.286 17 7675996 missense variant T/G snp 20
rs28934874 0.673 0.429 17 7675161 stop gained G/A,C,T snp 20
rs530941076 0.692 0.250 17 7674873 missense variant A/C,G,T snp 4.0E-06 20
rs587781525 0.679 0.429 17 7673778 missense variant T/A,C,G snp 20
rs730882008 0.692 0.321 17 7673775 stop gained C/A,G,T snp 4.0E-06 20
rs104894228 0.662 0.500 11 534286 missense variant C/A,G,T snp 19
rs1057519991 0.692 0.214 17 7675076 missense variant T/A,C,G snp 4.0E-06 19
rs1057520002 0.692 0.357 17 7674242 missense variant A/C,G snp 19
rs121912656 0.667 0.500 17 7674229 missense variant C/A,G,T snp 4.0E-06; 4.0E-06 19
rs121913500 0.615 0.464 2 208248388 missense variant C/A,G,T snp 4.0E-06 18
rs121913233 0.657 0.429 11 533874 missense variant T/A,C,G snp 18
rs121913273 0.638 0.357 3 179218294 missense variant G/A,C snp 18
rs1057519990 0.699 0.321 17 7673824 missense variant C/A,G,T snp 4.0E-06 18
rs764146326 0.679 0.429 17 7673779 missense variant C/A,G,T snp 4.0E-06 18
rs786201059 0.679 0.321 17 7673764 missense variant C/G,T snp 18
rs863224451 0.692 0.429 17 7673796 stop gained C/A,G,T snp 18
rs104894226 0.692 0.464 11 534285 missense variant C/A,G,T snp 17
rs28933406 0.667 0.429 11 533875 missense variant G/C,T snp 17
rs121913286 0.679 0.250 3 179218306 missense variant C/A,G snp 17
rs121909224 0.692 0.464 10 87933147 stop gained C/G,T snp 1.2E-05 17
rs1057519747 0.715 0.250 17 7675094 missense variant A/C,G,T snp 17
rs1057519981 0.715 0.321 17 7674251 stop lost A/C,G snp 17
rs1057520008 0.707 0.393 17 7674918 stop lost A/C,G,T snp 17
rs483352697 0.685 0.429 17 7674944 missense variant C/A,G,T snp 4.0E-06 17
rs587782329 0.692 0.250 17 7674217 missense variant C/A,G,T snp 17