Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1555738204 1.000 0.120 19 46755671 frameshift variant -/AGCCC delins 1
rs1555738245 1.000 0.120 19 46755717 frameshift variant G/AT delins 1
rs1555738311 1.000 0.120 19 46755794 frameshift variant GCGCC/- delins 1
rs1555738456 1.000 0.120 19 46755914 frameshift variant T/- del 1
rs1555738502 1.000 0.120 19 46755976 stop gained C/T snv 1
rs1555738568 1.000 0.120 19 46756012 frameshift variant -/CCCGC delins 1
rs1555738651 1.000 0.120 19 46756104 frameshift variant G/- delins 1
rs1555738675 1.000 0.120 19 46756131 frameshift variant GGCTGGGCGGTGCAGCTGCTGGACTTGACCTTCGC/- delins 1
rs1555738686 1.000 0.120 19 46756136 frameshift variant G/- del 1
rs1555738753 1.000 0.120 19 46756228 stop gained G/T snv 1
rs1555738764 1.000 0.120 19 46756244 frameshift variant G/-;GGG delins 1
rs1555738823 1.000 0.120 19 46756309 frameshift variant TTCGGCTGCAA/- del 1
rs1555738883 1.000 0.120 19 46756407 frameshift variant GC/- delins 1
rs1555739041 1.000 0.120 19 46756569 frameshift variant C/- del 1
rs1555739333 1.000 0.120 19 46756925 frameshift variant C/- del 1
rs28937901 1.000 0.120 19 46756396 missense variant C/A;T snv 6.0E-06 1
rs28937905 1.000 0.120 19 46755610 missense variant C/G;T snv 8.6E-06; 4.3E-06 1
rs398124395 1.000 0.120 19 46756391 missense variant C/A;T snv 6.1E-06 1
rs587777823 1.000 0.120 19 46755835 frameshift variant -/ACCT delins 1
rs587780334 1.000 0.120 19 46756477 stop gained G/C;T snv 8.4E-03; 9.0E-06 1
rs748087383 1.000 0.120 19 46756617 frameshift variant CG/- delins 8.2E-06 1
rs752731569 1.000 0.120 19 46755527 stop gained G/A;T snv 8.4E-06 7.0E-06 1
rs753811189 1.000 0.120 19 46756486 missense variant T/C;G snv 1
rs765885747 1.000 0.120 19 46756378 stop gained G/C;T snv 4.4E-05; 2.5E-05 1
rs768606230 1.000 0.120 19 46756834 missense variant C/T snv 9.0E-06 1.4E-05 1