Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1023835002 0.763 0.280 15 44711547 start lost A/G;T snv 10
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs104886003 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 71
rs104894226 0.658 0.560 11 534285 missense variant C/A;G;T snv 29
rs104894228 0.605 0.560 11 534286 missense variant C/A;G;T snv 48
rs104894229 0.564 0.600 11 534289 missense variant C/A;G;T snv 73
rs104894230 0.564 0.600 11 534288 missense variant C/A;G;T snv 73
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1056836 0.581 0.680 2 38071060 missense variant G/C snv 0.51 58
rs1057519747 0.716 0.280 17 7675094 missense variant A/C;G;T snv 23
rs1057519816 0.763 0.200 17 39711955 missense variant C/A;T snv 14
rs1057519847 0.570 0.560 7 55191821 missense variant CT/AG mnv 72
rs1057519848 0.570 0.560 7 55191822 missense variant TG/GT mnv 72
rs1057519877 0.763 0.280 15 44711549 start lost G/A snv 10
rs1057519879 0.763 0.280 15 44711548 start lost T/C;G snv 10
rs1057519881 0.776 0.240 9 21971111 missense variant T/C snv 8
rs1057519883 0.742 0.280 9 21971120 missense variant C/G;T snv 14
rs1057519895 0.724 0.240 4 152328232 missense variant C/A;G;T snv 17
rs1057519909 0.790 0.240 15 66435116 missense variant A/C snv 7
rs1057519920 0.790 0.160 2 177234232 missense variant C/A;G;T snv 7
rs1057519921 0.763 0.240 2 177234231 missense variant T/C snv 10
rs1057519922 0.790 0.200 2 177234082 missense variant C/G;T snv 7
rs1057519923 0.807 0.200 2 177234081 missense variant T/A snv 6
rs1057519924 0.807 0.200 2 177234080 missense variant C/A snv 6
rs1057519925 0.683 0.560 3 179210291 missense variant G/A;C snv 25