Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519959 0.882 0.200 11 66063028 missense variant A/C snv 4
rs754688962 0.851 0.200 2 197402637 missense variant T/C;G snv 5
rs786201419 0.790 0.160 17 7675180 missense variant C/A;T snv 8
rs1057519997 0.776 0.320 17 7676037 missense variant A/C;G;T snv 9
rs786203071 0.776 0.240 17 7675181 missense variant T/A;G snv 9
rs1057519926 0.776 0.200 3 179210293 missense variant A/T snv 10
rs886039484 0.641 0.440 17 7674888 missense variant T/C;G snv 10
rs1057520005 0.742 0.360 17 7673800 missense variant C/A;G snv 11
rs375874539 0.732 0.320 17 7674237 missense variant G/A;C snv 11
rs587780071 0.732 0.240 17 7674951 missense variant G/A snv 11
rs587782177 0.763 0.200 17 7674887 missense variant C/A;G;T snv 11
rs1057519999 0.763 0.160 17 7674247 missense variant T/C;G snv 12
rs1057520006 0.752 0.240 17 7673799 missense variant A/C;G;T snv 12
rs876660807 0.763 0.160 17 7674248 missense variant T/C snv 12
rs1057519975 0.649 0.480 17 7675209 missense variant A/C;G;T snv 13
rs587781991 0.724 0.240 17 7675208 missense variant C/A;T snv 14
rs121912655 0.724 0.400 17 7674238 missense variant C/A;G;T snv 15
rs121913495 0.672 0.400 20 58909366 missense variant G/A;T snv 15
rs786203436 0.701 0.280 17 7675125 missense variant A/C;G;T snv 15
rs1057519983 0.724 0.360 17 7673797 missense variant A/G snv 16
rs1057519985 0.724 0.360 17 7673763 missense variant T/A;C;G snv 16
rs942158624 0.724 0.320 17 7674948 missense variant T/A snv 16
rs967461896 0.724 0.240 17 7675086 missense variant A/C;G;T snv 16
rs1057519747 0.716 0.280 17 7675094 missense variant A/C;G;T snv 17
rs1057520007 0.701 0.440 17 7674917 missense variant T/A;C;G snv 17