Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs767910122 0.724 0.280 7 150948446 frameshift variant -/GTCCG ins 4.4E-05 17
rs794728489 7 150959670 frameshift variant -/CCAC ins 1
rs137854605 1.000 0.120 3 38581337 missense variant GA/TT mnv 2
rs794728508 1.000 0.120 7 150974864 frameshift variant A/- del 2
rs794728506 7 150974918 frameshift variant C/- del 1
rs794728448 0.724 0.280 7 150948445 frameshift variant CT/G delins 17
rs397508087 1.000 0.120 11 2588799 frameshift variant C/-;CC delins 2
rs794728425 1.000 0.120 7 150958220 frameshift variant -/GGCGATGGGAGCTGGCCGGG delins 2
rs794728470 1.000 0.120 7 150947367 frameshift variant -/TCGCCCCG delins 1.4E-05 2
rs397508101 11 2847812 inframe deletion CCA/- delins 1
rs794728426 7 150958163 frameshift variant CGCG/GCTTTT delins 1
rs794728428 7 150958116 frameshift variant TCGGCCG/- delins 1
rs794728434 7 150952777 frameshift variant -/CAGG delins 1
rs794728456 7 150947794 frameshift variant G/- delins 1
rs794728457 7 150947782 frameshift variant TCTCCCC/- delins 1
rs794728464 7 150947512 splice region variant -/CTGC delins 1
rs794728465 7 150947400 frameshift variant -/G delins 1
rs794728467 7 150947380 frameshift variant -/CCGCC;CGCC delins 1
rs794728472 7 150947344 frameshift variant G/- delins 1
rs794728476 7 150974765 inframe insertion -/ATCTGCGCG delins 1
rs794728497 7 150952840 frameshift variant C/- delins 1
rs794728499 7 150951578 frameshift variant G/- delins 1
rs794728500 7 150951013 frameshift variant G/- delins 1
rs794728507 7 150974912 frameshift variant C/- delins 1
rs794728563 11 2445260 frameshift variant GCCCGGCGCCCCAGGTCCCGCGC/- delins 1