Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1554698582 1.000 0.160 9 95477618 inframe deletion ACCAGCAGGACGCCA/- delins 1
rs368869806 0.614 0.480 9 95485875 splice acceptor variant C/T snv 4.0E-06 7.0E-06 97
rs1064793921 1.000 0.160 9 95476161 splice acceptor variant T/C;G snv 2
rs878853849 1.000 0.160 9 95506601 splice acceptor variant T/C;G snv 2
rs1060502271 1.000 0.160 9 95479149 splice acceptor variant T/A snv 1
rs1554698613 1.000 0.160 9 95477680 splice acceptor variant TTAGACAGGCATAGGCGAGCTGCAAGCAGAACAATGG/- delins 1
rs863224443 1.000 0.160 9 95449942 splice acceptor variant T/C snv 1
rs1057520590 1.000 0.160 9 95482204 splice acceptor variant C/G snv 1
rs1060502285 1.000 0.160 9 95456414 splice acceptor variant C/T snv 1
rs1564031259 1.000 0.160 9 95467400 splice acceptor variant AAAAAGGAAGATCACCACTACCTGGAACAGAAGAGGCACAAGGTCAGACCCCAG/- delins 1
rs878853852 1.000 0.160 9 95462000 splice acceptor variant T/A;C snv 1
rs1564051834 1.000 0.160 9 95478187 splice acceptor variant C/T snv 1
rs1554708795 1.000 0.160 9 95506574 splice acceptor variant GGCGCTTTCCGGCCAGTAGCCTTCCCCTGGGGACGAAGCAGA/- del 1
rs1131690984 9 95476859 splice acceptor variant T/G snv 1
rs1131691001 9 95449940 splice acceptor variant C/- delins 1
rs1085307752 9 95479148 splice acceptor variant C/A;T snv 1
rs1554691658 0.807 0.240 9 95459653 frameshift variant C/GGGTCCACAACATCT delins 11
rs863225055 0.925 0.160 9 95476760 frameshift variant AAAAGGGATTC/- delins 3
rs1060502292 1.000 0.160 9 95468803 frameshift variant AG/- delins 2
rs1060502273 1.000 0.160 9 95453562 frameshift variant AT/- del 2
rs1131690969 1.000 0.160 9 95480525 frameshift variant CTTT/- delins 2
rs1131690987 1.000 0.160 9 95480449 frameshift variant A/- del 2
rs863225467 1.000 0.160 9 95467134 frameshift variant AGTA/CT delins 2
rs1564032829 0.925 0.160 9 95468757 frameshift variant T/- delins 2
rs864622583 1.000 0.160 9 95506497 frameshift variant AACTTGCCGCAGTTTTTTTGAATGTAACAACCCAG/- delins 1