Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs72653706 0.695 0.480 16 16163078 stop gained G/A snv 1.4E-03 1.2E-03 32
rs5742904 0.689 0.280 2 21006288 missense variant C/A;T snv 2.8E-04 7.3E-04 22
rs121908029 0.763 0.200 19 11105588 stop gained G/A;C;T snv 1.6E-05; 1.6E-05; 8.1E-06 13
rs137929307 0.752 0.240 19 11116928 missense variant G/A snv 4.4E-05 4.9E-05 12
rs879254850 0.776 0.160 19 11113365 missense variant A/G;T snv 4.0E-06 9
rs374603772 0.776 0.160 1 55058630 missense variant C/T snv 4.4E-05 2.8E-05 9
rs78678589 0.925 0.160 16 16203457 missense variant G/C;T snv 1.6E-05 8
rs373371572 0.851 0.080 19 11116936 missense variant C/T snv 4.0E-06 2.8E-05 6
rs879255000 0.851 0.080 19 11116882 missense variant T/C;G snv 6
rs28362261 0.851 0.160 1 55058129 missense variant A/G snv 1.2E-03 4.8E-03 6
rs28941776 0.882 0.080 19 11116153 missense variant G/A;T snv 2.4E-05 5
rs754536745 0.882 0.080 19 11120144 missense variant G/A;T snv 2.0E-05 5
rs879254459 0.882 0.080 19 11102771 missense variant G/A snv 5
rs774439908 0.827 0.160 19 11113348 stop gained C/A;G;T snv 4.0E-06; 4.0E-06 5
rs777188764 0.882 0.080 19 11116874 missense variant G/A;T snv 3.2E-05; 1.6E-05 4
rs879254906 0.882 0.080 19 11113630 missense variant A/G snv 3
rs141502002 0.882 0.080 1 55058549 missense variant C/T snv 6.0E-04 2.8E-03 3
rs370507566 0.882 0.040 1 55057404 missense variant G/A;T snv 4.0E-05; 1.2E-05 3
rs771479424 0.882 0.120 1 55052764 stop gained A/G;T snv 1.2E-05 3
rs1032566999 0.925 0.080 22 41903099 missense variant C/T snv 1.1E-05 7.0E-06 2
rs995013832 1.000 1 55058617 missense variant G/T snv 4.0E-06 1.4E-05 1