Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1567572265 1.000 0.280 16 89282833 frameshift variant CT/- delins 1
rs1555528400 1.000 0.280 16 89282909 frameshift variant TT/- delins 1
rs886039734 1.000 0.280 16 89284364 frameshift variant TTGT/- delins 4.0E-06 1
rs863223320 1.000 0.280 16 89284237 frameshift variant A/- del 1
rs1555529979 1.000 0.280 16 89285565 frameshift variant C/- delins 1
rs1555525977 1.000 0.280 16 89280344 stop gained GA/TT mnv 1
rs1381957912 1.000 0.280 16 89279872 stop gained C/A;T snv 5.5E-06 1
rs863223321 1.000 0.280 16 89280588 frameshift variant TG/- delins 1
rs749201074 1.000 0.280 16 89284565 stop gained G/A;C snv 1.2E-05 7.0E-06 1
rs797045027 1.000 0.280 16 89284141 frameshift variant CTTT/- delins 1
rs1555527341 1.000 0.280 16 89281489 frameshift variant T/- del 1
rs761636251 1.000 0.280 16 89286064 stop gained G/A;T snv 8.0E-06 1
rs1567566026 1.000 0.280 16 89281477 frameshift variant G/- delins 1
rs1567579092 1.000 0.280 16 89284494 frameshift variant TT/- del 1
rs1057518663 1.000 0.280 16 89283420 stop gained G/T snv 1
rs1555529551 1.000 0.280 16 89284863 stop gained G/C snv 1
rs863223319 1.000 0.280 16 89274958 splice acceptor variant C/G;T snv 1
rs1555527929 1.000 0.280 16 89282254 stop gained T/A snv 1
rs1555529181 1.000 0.280 16 89284135 frameshift variant GAGT/- delins 1
rs863225296 1.000 0.280 16 89279362 stop gained G/A snv 1
rs761848111 1.000 0.280 16 89282980 stop gained G/A snv 1
rs749632782 1.000 0.280 16 89282336 stop gained G/A;C snv 2.0E-05 7.0E-06 1
rs1064794330 1.000 0.280 16 89283315 frameshift variant CTTT/- delins 1
rs1567583835 1.000 0.280 16 89285650 splice acceptor variant C/G snv 1
rs1567579525 1.000 0.280 16 89284594 stop gained G/A snv 1