Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs28939719 0.882 0.040 19 919563 missense variant T/C snv 2
rs374434303 0.882 0.200 19 7561509 missense variant C/A;T snv 3.8E-05 4
rs376239580 0.925 0.040 20 5302632 missense variant G/A snv 1.2E-05 2.1E-05 2
rs515726219 1.000 0.040 4 67754242 splice donor variant T/C snv 3.6E-05 7.0E-06 1
rs515726224 0.925 0.320 8 38417962 missense variant C/T snv 3
rs606231407 1.000 0.040 10 101770613 missense variant C/T snv 1.6E-05 2
rs727505367 1.000 0.040 4 67753986 missense variant A/C snv 1.4E-05 2
rs727505369 0.925 0.160 8 38424624 missense variant T/C snv 3
rs727505370 1.000 0.040 8 38414840 missense variant A/G snv 2
rs727505371 1.000 0.040 8 38421840 frameshift variant AG/- delins 4.0E-06 2
rs727505372 0.925 0.040 12 57013359 missense variant G/T snv 3
rs727505373 0.925 0.160 8 38429744 missense variant T/C snv 3
rs727505374 1.000 0.040 X 8539744 stop gained G/A snv 2
rs727505375 1.000 0.040 4 103658329 stop gained C/T snv 4.0E-06 7.0E-06 1
rs727505376 0.925 0.160 8 38414279 missense variant C/G;T snv 2
rs727505377 1.000 0.040 8 38414001 missense variant A/G snv 1
rs730882248 0.925 0.160 7 5711761 splice region variant C/T snv 2
rs74452732 0.851 0.160 4 67753825 missense variant C/A;T snv 4.0E-06 1
rs774317793 1.000 0.040 4 67754283 missense variant T/C snv 1.9E-04 2.1E-05 1
rs774526181 0.882 0.200 12 106427360 splice donor variant T/C snv 8.0E-06 2.1E-05 3
rs781328162 0.925 0.160 8 38413714 missense variant C/T snv 2.0E-05 3.5E-05 1
rs797044452 1.000 0.040 4 67744788 splice acceptor variant C/T snv 1
rs876661330 0.882 0.160 10 101771522 stop gained G/A snv 4.0E-06 2
rs886039799 0.763 0.320 7 33273896 frameshift variant C/- del 17
rs886907903 1.000 0.040 4 67754226 missense variant A/C snv 1