Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs530941076 0.695 0.280 17 7674873 missense variant A/C;G;T snv 4.0E-06 20
rs587781525 0.689 0.480 17 7673778 missense variant T/A;C;G snv 20
rs730882005 0.701 0.400 17 7674250 missense variant C/A;G;T snv 8.0E-06 20
rs764146326 0.662 0.480 17 7673779 missense variant C/A;G;T snv 4.0E-06 20
rs1057519991 0.662 0.440 17 7675076 missense variant T/A;C;G snv 4.0E-06 19
rs121913255 0.667 0.400 1 114713907 missense variant T/A;G snv 19
rs876660754 0.701 0.360 17 7675095 missense variant C/A;T snv 18
rs1057519747 0.716 0.280 17 7675094 missense variant A/C;G;T snv 17
rs1057519946 0.732 0.280 19 52212729 missense variant C/G;T snv 17
rs1057520007 0.701 0.440 17 7674917 missense variant T/A;C;G snv 17
rs587782329 0.677 0.280 17 7674217 missense variant C/A;G;T snv 16
rs985033810 0.724 0.280 17 7674232 missense variant C/A;G;T snv 16
rs1057519989 0.732 0.240 17 7674233 missense variant C/A;G;T snv 15
rs121912657 0.683 0.480 17 7673806 missense variant C/A;G;T snv 4.0E-06 15
rs876659802 0.732 0.440 17 7673787 missense variant G/A;C;T snv 15
rs1057519895 0.724 0.240 4 152328232 missense variant C/A;G;T snv 14
rs17849781 0.701 0.480 17 7673788 missense variant G/A;C;T snv 14
rs587782664 0.742 0.320 17 7674252 missense variant C/A;G;T snv 4.0E-06 14
rs867384286 0.732 0.240 4 152328233 missense variant G/A;C snv 4.3E-06 14
rs876660333 0.742 0.360 17 7673805 missense variant A/C;G;T snv 13
rs1057519896 0.742 0.320 4 152326136 missense variant C/A;T snv 12
rs1057519999 0.763 0.160 17 7674247 missense variant T/C;G snv 12