Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121909224 0.627 0.560 10 87933147 stop gained C/G;T snv 1.2E-05 35
rs121909231 0.667 0.600 10 87961095 stop gained C/A;T snv 29
rs121909219 0.689 0.400 10 87957915 stop gained C/A;T snv 24
rs28934908 0.732 0.280 X 154031409 missense variant G/A;T snv 5.5E-06 12
rs1085308043 0.763 0.200 10 87925511 splice acceptor variant A/G;T snv 12
rs112795301 0.776 0.160 3 70972634 stop gained G/A snv 11
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 8
rs863225082 0.827 0.160 6 43007265 missense variant G/A snv 7
rs878853161 0.851 0.240 1 42929977 frameshift variant AT/- del 7
rs727504317 0.807 0.320 15 66435145 missense variant G/A snv 6
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 6
rs2388334 0.882 0.040 6 98143746 intron variant A/G snv 0.39 5
rs1452075 1.000 0.040 3 62495388 intron variant C/T snv 0.73 4
rs797045050 0.807 0.120 2 240797715 missense variant C/T snv 4
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 4
rs762292772 0.882 0.160 22 50721505 frameshift variant G/-;GG delins 4
rs10741657 0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 3
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 3
rs1565532385 0.925 0.080 11 118374964 frameshift variant CA/- del 3
rs11787216 1.000 0.040 8 141605122 intron variant C/T snv 0.26 2
rs13294439 1.000 0.040 9 23358877 intron variant A/C snv 0.32 2
rs4307059 0.882 0.080 5 25967594 intron variant T/A;C snv 2
rs886037776 0.925 0.280 9 137817477 stop gained G/A snv 2
rs526126 1.000 0.040 11 61857413 intron variant G/C;T snv 0.81; 8.0E-06 2
rs4588
GC
0.597 0.720 4 71752606 missense variant G/A;T snv 1.6E-05; 0.25 2