Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104894229 0.564 0.600 11 534289 missense variant C/A;G;T snv 52
rs121913281 0.623 0.520 3 179234296 missense variant C/T snv 37
rs104894230 0.564 0.600 11 534288 missense variant C/A;G;T snv 36
rs104894228 0.605 0.560 11 534286 missense variant C/A;G;T snv 30
rs121913274 0.645 0.320 3 179218304 missense variant A/C;G;T snv 28
rs397516436 0.641 0.440 17 7674894 stop gained G/A;C snv 26
rs28934575 0.641 0.400 17 7674230 missense variant C/A;G;T snv 25
rs121909219 0.689 0.400 10 87957915 stop gained C/A;T snv 24
rs786201057 0.677 0.400 17 7675995 missense variant G/A;C;T snv 24
rs104894226 0.658 0.560 11 534285 missense variant C/A;G;T snv 23
rs1057519925 0.683 0.560 3 179210291 missense variant G/A;C snv 23
rs121909229 0.683 0.400 10 87933148 missense variant G/A;C;T snv 23
rs786201838 0.683 0.440 17 7674953 missense variant T/A;C;G snv 23
rs1057519932 0.683 0.320 3 179234298 missense variant T/G snv 22
rs876658468 0.689 0.440 17 7674954 missense variant G/A;C;T snv 22
rs121913273 0.605 0.440 3 179218294 missense variant G/A;C snv 21
rs193920774 0.695 0.440 17 7673823 missense variant C/A;T snv 21
rs28934874 0.695 0.480 17 7675161 missense variant G/A;C;T snv 21
rs876660821 0.689 0.400 17 7675075 missense variant A/C;G;T snv 21
rs1057519981 0.689 0.440 17 7674251 missense variant A/C;G;T snv 20
rs1057520002 0.695 0.360 17 7674242 missense variant A/C;G snv 20
rs1057520003 0.695 0.320 17 7675996 missense variant T/G snv 20
rs121913233 0.627 0.520 11 533874 missense variant T/A;C;G snv 20
rs121913286 0.677 0.280 3 179218306 missense variant C/A;G snv 20
rs587781525 0.689 0.480 17 7673778 missense variant T/A;C;G snv 20