Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs1057519991 0.662 0.440 17 7675076 missense variant T/A;C;G snv 4.0E-06 26
rs121913275 0.672 0.320 3 179218305 missense variant G/A;C;T snv 4.0E-06 26
rs138729528 0.677 0.480 17 7675089 missense variant G/A;C snv 1.6E-05 25
rs121912657 0.683 0.480 17 7673806 missense variant C/A;G;T snv 4.0E-06 24
rs121913338 0.677 0.400 7 140753354 missense variant T/A;C;G snv 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
rs121909229 0.683 0.400 10 87933148 missense variant G/A;C;T snv 23
rs121913286 0.677 0.280 3 179218306 missense variant C/A;G snv 23
rs730882008 0.683 0.440 17 7673775 missense variant C/A;G;T snv 4.0E-06 23
rs1057519932 0.683 0.320 3 179234298 missense variant T/G snv 22
rs1057519981 0.689 0.440 17 7674251 missense variant A/C;G;T snv 22
rs11554273 0.689 0.240 20 58909365 missense variant C/A;G;T snv 4.0E-06 22
rs17849781 0.701 0.480 17 7673788 missense variant G/A;C;T snv 22
rs193920774 0.695 0.440 17 7673823 missense variant C/A;T snv 22
rs876660821 0.689 0.400 17 7675075 missense variant A/C;G;T snv 22
rs1057520007 0.701 0.440 17 7674917 missense variant T/A;C;G snv 21
rs28934874 0.695 0.480 17 7675161 missense variant G/A;C;T snv 21
rs483352697 0.695 0.480 17 7674944 missense variant C/A;G;T snv 4.0E-06 21
rs530941076 0.695 0.280 17 7674873 missense variant A/C;G;T snv 4.0E-06 21