Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs758946412 0.790 0.240 X 100407507 frameshift variant G/-;GG delins 12
rs1555985372 1.000 X 100407591 frameshift variant -/C delins 2
rs191333060 1.000 0.040 X 100296405 missense variant G/A;C snv 1.3E-03 1
rs1569315842 1.000 0.080 X 100408107 frameshift variant -/G delins 1
rs796052839 0.882 0.200 X 100407579 missense variant T/C;G snv 1
rs1131691646 1.000 0.200 X 100407077 frameshift variant G/-;GG delins 1
rs863224907 1.000 0.200 X 100408140 missense variant GC/AT mnv 1
rs587784299 1.000 0.200 X 100407903 missense variant T/A;C snv 1
rs1555985163 1.000 0.200 X 100407150 frameshift variant CCAGGTC/- delins 1
rs1569315876 1.000 0.200 X 100408136 stop gained G/C snv 1
rs1569314475 1.000 0.200 X 100406922 frameshift variant T/- delins 1
rs1555985639 1.000 0.200 X 100408108 stop gained GC/AT mnv 1
rs267606933 1.000 0.200 X 100406927 missense variant G/A;C snv 1
rs1569315231 1.000 0.200 X 100407680 stop gained G/C snv 1
rs1569315169 1.000 0.200 X 100407627 frameshift variant T/- delins 1
rs1569314809 1.000 0.200 X 100407256 missense variant C/A snv 1
rs1057521256 1.000 0.200 X 100406783 stop gained G/A;C snv 1
rs1555985543 1.000 0.200 X 100407979 frameshift variant G/- delins 1
rs1569315156 1.000 0.200 X 100407604 frameshift variant C/- delins 1
rs1555985105 1.000 0.200 X 100407043 stop gained G/A snv 1
rs132630323 1.000 0.200 X 100407276 missense variant A/T snv 1
rs1569315042 1.000 0.200 X 100407476 frameshift variant GA/- delins 1
rs769967221 1.000 0.200 X 100407415 stop gained G/A;T snv 1
rs201989363 1.000 0.200 X 100406898 missense variant G/A;C;T snv 4.4E-05 1
rs1569314152 1.000 0.200 X 100406567 frameshift variant -/A delins 1