Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104894483 0.925 0.120 15 68214373 stop gained C/A;G;T snv 6.8E-05; 2.6E-03; 2.0E-05; 4.0E-06 3
rs397515352 0.925 0.120 15 68211844 frameshift variant -/G delins 2.4E-05; 2.8E-05 3
rs587779408 0.882 0.160 11 6391804 missense variant G/A snv 2.4E-05 2.8E-05 3
rs121908080 0.925 0.120 15 68211698 inframe deletion ATG/- delins 2
rs154774633 0.925 0.120 15 68214387 missense variant A/G snv 2
rs154774636 0.925 0.120 15 68229568 missense variant C/G snv 2
rs154774640 0.925 0.120 15 68218584 stop gained G/C snv 8.0E-06 2.1E-05 2
rs751486476 0.925 0.160 15 68218549 missense variant C/T snv 4.0E-06 2
rs756522171 1.000 0.120 15 68211674 splice donor variant C/T snv 1.2E-05 2
rs768422260 0.925 0.120 15 68208280 inframe deletion GAG/- delins 1.4E-05 2
rs774543080 0.925 0.120 15 68211765 frameshift variant AG/- delins 8.0E-06 2
rs104894484 1.000 0.120 15 68211793 missense variant C/T snv 1
rs104894486 1.000 0.120 15 68209639 stop gained G/A;C snv 1
rs1194940137 1.000 0.120 15 68208187 missense variant G/T snv 4.0E-06 1
rs121908079 1.000 0.120 15 68211289 inframe deletion ATA/- delins 1
rs1381427322 1.000 0.120 15 68229502 missense variant C/T snv 1.2E-05 1
rs150363441 1.000 0.120 15 68208301 missense variant C/A;G;T snv 2.4E-05 1
rs154774639 1.000 0.120 15 68208186 frameshift variant G/- delins 1.4E-05 1
rs1555438212 1.000 0.120 15 68208239 stop gained C/T snv 1
rs1555438229 1.000 0.120 15 68208288 frameshift variant -/AG delins 1
rs1555438234 1.000 0.120 15 68208306 frameshift variant TGTCC/- delins 1
rs1555438255 1.000 0.120 15 68208354 missense variant A/G snv 1
rs1555438411 1.000 0.120 15 68209637 stop gained C/T snv 1
rs1555438443 1.000 0.120 15 68209759 stop gained C/T snv 1
rs1555438614 1.000 0.120 15 68211262 splice donor variant C/A snv 1