Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913482 0.630 0.680 4 1801837 missense variant C/T snv 45
rs28933068 0.645 0.560 4 1805644 missense variant C/A;G;T snv 1.6E-05 30
rs121913105 0.653 0.600 4 1806163 missense variant A/C;T snv 30
rs78311289 0.689 0.440 4 1806162 missense variant A/C;G snv 4.0E-06 25
rs1400419650 0.708 0.320 14 92005938 stop gained C/A;T snv 4.0E-06 1.4E-05 38
rs1555386022 0.708 0.320 14 92003418 splice donor variant C/A snv 38
rs121918130 0.716 0.360 9 136433182 missense variant G/A;T snv 3.4E-05; 4.2E-06 18
rs66527965 0.763 0.240 17 50193038 missense variant C/A;T snv 31
rs1014959895 0.763 0.360 16 68329105 stop gained G/C;T snv 4.0E-06; 1.6E-05 16
rs1251713297 0.776 0.360 16 68355785 stop gained C/A snv 8.1E-06 15
rs121912633 0.790 0.240 12 109792396 missense variant C/A;T snv 4.0E-06 10
rs587777512 0.827 0.320 4 150583180 missense variant C/G;T snv 7
rs886041093 0.827 0.280 9 137815998 missense variant G/A snv 7
rs77975504 0.827 0.280 12 109792695 missense variant C/T snv 6
rs749621890 0.851 0.040 8 28717012 missense variant C/G;T snv 4.0E-06; 4.0E-06 7
rs121912637 0.851 0.160 12 109784378 missense variant G/A;C snv 5
rs267607149 0.851 0.120 12 109784385 missense variant C/T snv 5
rs387906904 0.851 0.080 12 109803009 missense variant G/A snv 5
rs369634007 0.882 0.080 2 112098688 missense variant A/G snv 1.6E-05 2.1E-05 10
rs864309531 0.882 0.400 2 216423668 stop gained G/T snv 5
rs267607148 0.882 0.120 12 109800639 missense variant C/T snv 4
rs774568856 0.882 0.200 6 83174481 missense variant A/G snv 1.7E-05 7.0E-06 4
rs121912632 0.882 0.080 12 109792407 missense variant C/T snv 3
rs181011657 0.882 0.120 11 103257719 stop gained C/T snv 6.8E-05 1.4E-04 3
rs759549373 0.925 0.080 11 103253342 missense variant G/A;T snv 6.0E-05; 4.0E-06 4