Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1555392032 1.000 15 38339805 frameshift variant -/A delins 3
rs1555386654 1.000 0.080 15 38253209 frameshift variant T/- del 1
rs1555392609 1.000 0.080 15 38349515 stop gained C/T snv 1
rs1555392750 1.000 0.080 15 38351208 frameshift variant -/TA delins 1
rs1555391053 1.000 0.080 15 38322336 frameshift variant -/A delins 1
rs1057518683 1.000 0.080 15 38351302 stop gained C/T snv 1
rs750777752 1.000 0.080 15 38299392 stop gained C/A;G;T snv 4.0E-06 1
rs121434315 1.000 0.080 15 38299530 stop gained C/T snv 1
rs1057517941 1.000 0.080 15 38299386 stop gained C/T snv 7.0E-06 1
rs121434312 1.000 0.080 15 38322382 stop gained C/T snv 1
rs121434317 1.000 0.080 15 38351113 stop gained A/T snv 1
rs1566867209 1.000 0.080 15 38322261 frameshift variant -/A delins 1
rs1566876954 1.000 0.080 15 38351379 frameshift variant A/- delins 1
rs1555392759 1.000 0.080 15 38351250 frameshift variant CT/- delins 1
rs864622410 1.000 0.080 15 38351125 frameshift variant AT/- del 1
rs1555389690 1.000 0.080 15 38299443 stop gained G/T snv 1
rs1566868022 1.000 0.080 15 38324766 frameshift variant -/C delins 1
rs121434313 1.000 0.080 15 38299410 stop gained C/T snv 7.0E-06 1
rs878855228 1.000 0.080 15 38351478 frameshift variant AG/- delins 1
rs1555392783 1.000 0.080 15 38351424 frameshift variant AGTT/- delins 1
rs1566867246 1.000 0.080 15 38322332 frameshift variant CTTACGT/- delins 1
rs121434316 1.000 0.080 15 38349476 stop gained C/T snv 1
rs1566868058 1.000 0.080 15 38324810 splice donor variant G/A snv 1
rs1555391061 1.000 0.080 15 38322373 frameshift variant AG/- delins 1
rs121434318 1.000 0.080 15 38299471 missense variant T/A snv 1