Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs375002796 0.851 0.160 7 76058047 missense variant C/T snv 5.2E-05 2.8E-05 7
rs796052676 0.807 0.200 8 132180246 missense variant G/A snv 7
rs61748421 0.807 0.200 X 154031326 stop gained G/A;T snv 6
rs1057518786 1.000 6 33441374 splice region variant G/A snv 5
rs1057519444 0.925 0.120 22 32518208 missense variant GG/AA mnv 5
rs1057519567 0.882 0.040 7 76063554 frameshift variant G/- delins 5
rs1131692228 0.925 0.160 7 100646637 missense variant C/T snv 5
rs377619533 1.000 18 33743312 stop gained C/A;T snv 2.8E-05 5
rs587777623 0.882 0.120 11 686986 missense variant G/A snv 4.0E-06 5
rs145999922 0.882 0.040 2 227699378 missense variant A/G snv 4.4E-05 4.2E-05 4
rs397514627 0.882 0.160 10 73842486 missense variant C/A;G snv 4
rs750371878 0.925 6 104796666 stop gained G/A snv 4.0E-06 1.4E-05 4
rs775835429 0.925 0.040 2 227702236 frameshift variant -/TC delins 2.4E-05 2.1E-05 4
rs1555736565 0.925 0.080 19 13230191 missense variant C/A;T snv 3
rs778899140 0.925 6 165450268 missense variant T/C snv 4.0E-06 3