Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs368869806 0.614 0.480 9 95485875 splice acceptor variant C/T snv 4.0E-06 7.0E-06 97
rs755103500 0.851 0.160 9 95516820 start lost T/C;G snv 8.4E-06; 4.2E-06 4
rs766905791 0.851 0.160 9 95485815 start lost T/C snv 1.2E-05 4
rs1131690985 0.925 0.200 9 95449891 missense variant C/T snv 3
rs587776689 0.882 0.160 9 95453587 missense variant T/A;G snv 3
rs863225055 0.925 0.160 9 95476760 frameshift variant AAAAGGGATTC/- delins 3
rs1060502292 1.000 0.160 9 95468803 frameshift variant AG/- delins 2
rs1564032829 0.925 0.160 9 95468757 frameshift variant T/- delins 2
rs766313615 1.000 0.160 9 95467368 stop gained G/A;C;T snv 8.0E-06 2
rs1060502273 1.000 0.160 9 95453562 frameshift variant AT/- del 2
rs1060502281 1.000 0.160 9 95481954 stop gained G/T snv 2
rs1060502301 1.000 0.160 9 95458029 stop gained C/T snv 2
rs1064793921 1.000 0.160 9 95476161 splice acceptor variant T/C;G snv 2
rs1131690969 1.000 0.160 9 95480525 frameshift variant CTTT/- delins 2
rs1131690986 1.000 0.160 9 95485866 stop gained G/A snv 2
rs1131690987 1.000 0.160 9 95480449 frameshift variant A/- del 2
rs1249050389 0.925 0.240 9 95485696 stop gained G/C snv 2
rs863225054 1.000 0.160 9 95477548 missense variant T/C snv 2
rs878853849 1.000 0.160 9 95506601 splice acceptor variant T/C;G snv 2
rs863225467 1.000 0.160 9 95467134 frameshift variant AGTA/CT delins 2
rs1060502274 1.000 0.160 9 95469119 stop gained G/A snv 1
rs1554692291 1.000 0.160 9 95461940 stop gained G/C snv 1
rs1554695039 1.000 0.160 9 95468939 stop gained G/A snv 1
rs1564031259 1.000 0.160 9 95467400 splice acceptor variant AAAAAGGAAGATCACCACTACCTGGAACAGAAGAGGCACAAGGTCAGACCCCAG/- delins 1
rs1564035949 1.000 0.160 9 95469896 frameshift variant A/- delins 1