Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519951 0.882 0.080 3 49375472 missense variant C/G;T snv 4
rs121912664 0.630 0.320 17 7670699 missense variant C/A;G;T snv 1.2E-05 7
rs1057519928 0.807 0.200 3 179221147 missense variant A/C snv 8
rs786201419 0.790 0.160 17 7675180 missense variant C/A;T snv 8
rs786203071 0.776 0.240 17 7675181 missense variant T/A;G snv 8
rs1057519929 0.776 0.320 3 179199066 missense variant G/A snv 9
rs1057519941 0.776 0.240 3 179203761 missense variant T/C;G snv 9
rs1057519947 0.790 0.160 19 52212730 missense variant G/A snv 9
rs1057519987 0.776 0.280 17 7673810 missense variant A/C snv 9
rs867262025 0.790 0.360 3 179221146 missense variant G/A snv 9
rs1057519816 0.763 0.200 17 39711955 missense variant C/A;T snv 10
rs1057519926 0.776 0.200 3 179210293 missense variant A/T snv 10
rs1057519938 0.776 0.160 3 179203764 missense variant A/C;T snv 10
rs1057519939 0.776 0.160 3 179203763 missense variant A/C snv 10
rs1057519986 0.776 0.240 17 7673811 missense variant A/C;G snv 10
rs1057519988 0.776 0.240 17 7673812 missense variant A/C;G;T snv 10
rs121913284 0.776 0.160 3 179203765 missense variant T/A;G snv 10
rs1057519933 0.790 0.240 3 179199156 missense variant A/G snv 11
rs1057519934 0.790 0.240 3 179199158 missense variant G/C snv 11
rs1057519935 0.790 0.240 3 179199157 missense variant A/G snv 11
rs1057519936 0.776 0.200 3 179234284 missense variant A/G;T snv 11
rs1057519937 0.776 0.200 3 179234285 missense variant T/C snv 11
rs1057520004 0.752 0.240 17 7674884 missense variant A/C;T snv 11
rs121913287 0.752 0.400 3 179199088 missense variant G/A snv 11
rs121913496 0.724 0.440 11 533873 missense variant C/A;G;T snv 11