Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1567318022 1.000 0.120 16 3793539 frameshift variant -/T delins 1
rs1555473499 0.925 0.120 16 3738605 missense variant A/G snv 3
rs1555910114 1.000 0.120 22 41157167 splice acceptor variant A/G snv 1
rs1555470631 1.000 0.120 16 3727471 stop lost AAACGGAAAAAAAAGAACCCCCCCCACCCCCCCGCCAAAAAAAAACCAAAGAGAGAGACCAGATATTTAAATCAACTGGTTTTTAACAAAAAAATATATTCTTTGTATTGTTTCTTTAAACATCAATCCACCCTTCCATGGCTCGGAAGTCGCAGTTCCATCTAGGAATAAAAAGAACCTAGATGCCTGGATTTTCAGTACAAAAGGTCCAAGAACATGAAAGGGAAAAGGTGATGCTCTCACAATGCTACAAGCCCTCCACAAACTTCTCTAGCGTGTCCCCCGTGGTGTCCCCGACCAGGGACAGTTCGCTGGA/G delins 1
rs1567309482 1.000 0.120 16 3782694 frameshift variant AG/- delins 1
rs869312714 0.925 0.120 16 3729810 missense variant C/A snv 3
rs587783480 0.925 0.120 16 3758853 splice donor variant C/A snv 2
rs886041048 1.000 0.120 16 3739725 splice acceptor variant C/A snv 1
rs1555483834 0.925 0.120 16 3778699 splice donor variant C/A;T snv 2
rs121434626 1.000 0.120 16 3740399 missense variant C/G snv 1
rs200782888 0.925 0.120 16 3749626 splice donor variant C/G;T snv 2
rs267606752 0.925 0.120 16 3749631 missense variant C/T snv 2
rs587783483 0.925 0.120 16 3751725 splice donor variant C/T snv 2
rs1555472938 0.925 0.120 16 3736119 frameshift variant CA/- delins 2
rs1567316655 1.000 0.120 16 3792030 frameshift variant CA/- delins 1
rs1555473122 1.000 0.120 16 3736772 inframe deletion CCT/- delins 1
rs1567263114 0.925 0.120 16 3729405 frameshift variant CT/- delins 2
rs1555483716 1.000 0.120 16 3778093 frameshift variant G/- del 1
rs587783507 0.925 0.120 16 3729210 frameshift variant G/-;GG delins 2
rs1302427305 0.925 0.120 16 3792074 stop gained G/A snv 2
rs587783461 0.925 0.120 16 3793446 stop gained G/A snv 2
rs587783464 0.925 0.120 16 3792041 stop gained G/A snv 2
rs587783490 0.925 0.120 16 3740454 stop gained G/A snv 2
rs121434625 0.925 0.120 16 3793533 stop gained G/A snv 1
rs1567262537 1.000 0.120 16 3729142 stop gained G/A snv 1