Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1131691762 1.000 0.120 21 34449622 frameshift variant -/A delins 4.0E-06 1
rs1554425284 1.000 0.120 7 150950347 frameshift variant -/A delins 1
rs1554426219 1.000 0.120 7 150952646 frameshift variant -/A delins 1
rs1554431441 1.000 0.120 7 150977847 frameshift variant -/A delins 1
rs397508105 1.000 0.120 11 2847865 frameshift variant -/A delins 1
rs1554424083 1.000 0.120 7 150947383 frameshift variant -/ACCCG delins 1
rs863224478 1.000 0.120 7 150958473 splice acceptor variant -/AGCTTCAGGCGGAAGGTCTTGGCGCGGCC delins 1
rs794728458 1.000 0.120 7 150947785 frameshift variant -/C delins 1
rs397508117 0.925 0.120 11 2570712 frameshift variant -/G delins 2
rs1464992494 1.000 0.120 11 2847874 frameshift variant -/G delins 1
rs786204101 1.000 0.120 7 150947670 frameshift variant -/G delins 1
rs1554424079 1.000 0.120 7 150947381 frameshift variant -/GC delins 1
rs1554958132 1.000 0.120 11 2445478 frameshift variant -/GC delins 1
rs794728449 1.000 0.120 7 150947842 frameshift variant -/GCCCC delins 1
rs794728425 1.000 0.120 7 150958220 frameshift variant -/GGCGATGGGAGCTGGCCGGG delins 2
rs767910122 0.724 0.280 7 150948446 frameshift variant -/GTCCG ins 4.4E-05 17
rs1399804251 1.000 0.120 7 150948443 inframe insertion -/GTGTCC delins 1
rs1554424671 1.000 0.120 7 150948478 frameshift variant -/T delins 1
rs1554425527 1.000 0.120 7 150951065 stop gained -/T delins 1
rs1060500662 1.000 0.120 7 150950200 frameshift variant -/TC delins 1
rs794728470 1.000 0.120 7 150947367 frameshift variant -/TCGCCCCG delins 1.4E-05 2
rs794728508 1.000 0.120 7 150974864 frameshift variant A/- del 2
rs1563161538 1.000 0.120 7 150952843 frameshift variant A/- del 1
rs397508083 1.000 0.120 11 2588719 frameshift variant A/-;AA delins 7.0E-06 1
rs1564820729 1.000 0.120 11 2572011 splice acceptor variant A/C snv 1