Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1553920379 0.776 0.160 4 101032294 frameshift variant -/AGTA delins 27
rs1043614377 1.000 0.040 10 103049727 missense variant G/A snv 2
rs1562159088 1.000 0.040 6 110100644 stop gained G/A snv 2
rs786205232 0.925 0.040 1 110603893 missense variant C/T snv 4.0E-06 5
rs886041874 1.000 0.040 1 119721323 splice donor variant T/C snv 4.0E-06 2
rs764618040 1.000 0.040 1 119726868 missense variant C/T snv 1.6E-05 2.1E-05 2
rs587776508 0.882 0.040 12 123253922 frameshift variant T/- del 4.0E-06 4
rs1057519538 1.000 0.040 9 127651622 inframe deletion AAA/- del 1
rs1057518985 1.000 0.040 9 127673233 missense variant C/A;T snv 1
rs796053366 0.925 0.040 9 127673250 stop gained C/T snv 2
rs796053367 0.925 0.040 9 127675909 missense variant C/T snv 2
rs1057519539 1.000 0.040 9 127678479 stop gained G/A;T snv 1
rs1057519537 1.000 0.040 9 127682423 stop gained G/A snv 1
rs869312702 0.827 0.160 9 128203609 missense variant G/A snv 10
rs796053335 1.000 0.040 9 128632280 protein altering variant -/GCATGC delins 1
rs121909323 0.790 0.160 19 13277122 stop gained G/A snv 8
rs786200962 0.827 0.120 19 13298768 frameshift variant A/- del 7
rs1064794262 0.925 0.040 19 13303831 frameshift variant CT/- del 3
rs28934908 0.732 0.280 X 154031409 missense variant G/A;T snv 5.5E-06 23
rs587777308 0.763 0.040 5 161873196 missense variant G/A snv 14
rs727503940 1.000 0.040 5 161882638 missense variant C/A;T snv 1
rs796052491 0.851 0.040 5 161890982 missense variant T/A;C snv 4
rs1060499553 0.827 0.040 5 161890983 missense variant G/A snv 6
rs796052493 0.851 0.040 5 161895668 missense variant G/A;T snv 4
rs747138999 1.000 0.040 5 161895753 missense variant G/T snv 2