Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs758361736 0.776 0.240 15 89649836 missense variant T/G snv 1.3E-05 1.4E-05 16
rs778139192 0.776 0.360 15 89629561 stop gained G/A;T snv 4.1E-06; 7.3E-05 14
rs28933372 0.827 0.120 7 41966273 missense variant C/G snv 5
rs180758272 0.882 0.080 15 89649809 missense variant C/T snv 1.1E-04 5.2E-04 3
rs886039282 0.882 0.280 15 89630426 missense variant T/C snv 3
rs1235928535 0.925 0.160 15 89652864 stop gained G/A snv 6.8E-06 7.0E-06 2
rs138410949 0.925 0.120 15 89631625 missense variant T/C snv 1.6E-03 2.0E-03 2
rs752248403 0.925 0.080 15 89631709 frameshift variant GC/- del 6.5E-06 6.3E-05 2
rs146626238 1.000 0.080 15 89631647 missense variant C/T snv 1.2E-04 5.6E-04 1
rs1555424505 1.000 0.080 15 89645040 stop gained C/A snv 1
rs1555424684 1.000 0.080 15 89646974 frameshift variant -/G delins 1
rs1555425036 1.000 0.080 15 89649842 inframe deletion ATGTAC/- delins 1
rs202229910 1.000 0.080 15 89631689 stop gained G/A;C snv 1.2E-05; 1.1E-04 1
rs387907044 1.000 0.080 15 89649810 stop gained G/A;C snv 6.4E-06 1
rs387907045 1.000 0.080 15 89631605 stop gained G/A snv 1
rs569323391 1.000 0.080 15 89652774 stop gained G/A;C snv 7.0E-06 1
rs774403667 1.000 0.080 15 89633269 splice region variant G/C snv 1.2E-05 2.1E-05 1
rs797044463 1.000 0.080 15 89649309 frameshift variant -/A delins 7.0E-05 1
rs797044464 1.000 0.080 15 89649210 frameshift variant C/- delins 1
rs797045093 1.000 0.080 15 89631662 stop gained C/A snv 5.9E-06 7.0E-06 1
rs1567057019 1.000 0.080 15 89629123 splice acceptor variant C/G snv 1
rs202195179 1.000 0.080 15 89629527 stop gained G/A;C;T snv 2.0E-05; 3.2E-05; 4.0E-06 1