Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1060503625 0.882 0.080 14 95091289 missense variant G/A snv 3
rs875989784 0.925 0.080 14 95096510 frameshift variant AAGA/- delins 3
rs1131691192 1.000 0.040 14 95105784 splice acceptor variant C/A snv 2
rs1131691197 1.000 0.040 14 95096461 frameshift variant -/T delins 2
rs137852977 1.000 0.040 14 95117624 stop gained C/A;G snv 2
rs137852978 1.000 0.040 14 95106198 stop gained G/A snv 2
rs34678453 1.000 0.040 14 95099856 frameshift variant G/-;GG delins 2
rs754081635 1.000 0.040 14 95113166 stop gained G/A;C snv 4.0E-06 2
rs754818927 1.000 0.040 14 95115704 stop gained G/A;C snv 4.0E-06; 4.0E-06 2
rs765059994 1.000 0.040 14 95099779 splice donor variant C/A;G snv 2
rs875989779 0.925 0.080 14 95096166 stop gained G/C snv 2
rs875989780 0.925 0.080 14 95094149 stop gained G/C;T snv 2
rs878855246 1.000 0.040 14 95113106 stop gained G/A snv 2
rs886037667 1.000 0.040 14 95124428 stop gained C/A;T snv 4.0E-06 2
rs886037668 1.000 0.040 14 95124385 frameshift variant TCA/G delins 2
rs886037671 1.000 0.040 14 95117723 stop gained C/A snv 2
rs886037672 1.000 0.040 14 95116680 stop gained G/A snv 2
rs886037678 1.000 0.040 14 95115787 frameshift variant G/- del 2
rs886037679 1.000 0.040 14 95115746 frameshift variant -/CT ins 2
rs886037680 1.000 0.040 14 95115691 frameshift variant ATTG/- delins 2
rs886037683 1.000 0.040 14 95113091 splice donor variant C/A;T snv 2
rs886037684 1.000 0.040 14 95112226 stop gained G/A snv 7.0E-06 2
rs886037685 1.000 0.040 14 95111414 frameshift variant CA/- delins 2
rs886037687 1.000 0.040 14 95111329 stop gained GC/TT mnv 2
rs886037689 1.000 0.040 14 95111326 stop gained G/T snv 2