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
rs796052839 0.882 0.200 X 100407579 missense variant T/C;G snv 3
rs1057521256 1.000 0.200 X 100406783 stop gained G/A;C snv 1
rs1060502175 1.000 0.200 X 100402799 frameshift variant T/- delins 1
rs1060502176 1.000 0.200 X 100407891 missense variant G/A;C snv 1
rs1131691646 1.000 0.200 X 100407077 frameshift variant G/-;GG delins 1
rs132630323 1.000 0.200 X 100407276 missense variant A/T snv 1
rs132630324 1.000 0.200 X 100408345 stop gained G/A snv 1
rs132630325 1.000 0.200 X 100406586 stop gained G/C snv 1
rs132630326 1.000 0.200 X 100408456 stop gained C/A;T snv 1
rs1555984453 1.000 0.200 X 100402687 frameshift variant T/- del 1
rs1555985105 1.000 0.200 X 100407043 stop gained G/A snv 1
rs1555985163 1.000 0.200 X 100407150 frameshift variant CCAGGTC/- delins 1
rs1555985416 1.000 0.200 X 100407718 frameshift variant -/GGTCG delins 1
rs1555985448 1.000 0.200 X 100407813 missense variant G/T snv 1
rs1555985475 1.000 0.200 X 100407897 missense variant T/C snv 1
rs1555985543 1.000 0.200 X 100407979 frameshift variant G/- delins 1
rs1555985639 1.000 0.200 X 100408108 stop gained GC/AT mnv 1
rs1555985780 1.000 0.200 X 100408330 missense variant C/G snv 1
rs1555985820 1.000 0.200 X 100408459 stop gained GC/AA mnv 1
rs1569314152 1.000 0.200 X 100406567 frameshift variant -/A delins 1
rs1569314475 1.000 0.200 X 100406922 frameshift variant T/- delins 1
rs1569314809 1.000 0.200 X 100407256 missense variant C/A snv 1
rs1569315042 1.000 0.200 X 100407476 frameshift variant GA/- delins 1
rs1569315156 1.000 0.200 X 100407604 frameshift variant C/- delins 1