Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913482 0.685 0.393 4 1801837 missense variant C/T snp 30
rs66527965 0.801 0.179 17 50193038 missense variant C/A,T snp 29
rs78311289 0.662 0.357 4 1806162 missense variant A/C,G snp 4.0E-06 27
rs121913105 0.724 0.179 4 1806163 missense variant A/C,T snp 16
rs1014959895 0.801 0.286 16 68329105 stop gained G/C,T snp 4.0E-06; 1.6E-05 15
rs28933068 0.784 0.107 4 1805644 stop gained C/A,G,T snp 1.6E-05 11
rs121912633 0.801 0.179 12 109792396 missense variant C/A,T snp 4.0E-06 3.2E-05 10
rs587777512 0.821 0.286 4 150583180 missense variant C/G,T snp 6
rs387906904 0.821 0.071 12 109803009 missense variant G/A snp 6
rs587777511 0.846 0.286 4 150583181 missense variant G/A snp 5
rs121912637 0.878 0.107 12 109784378 missense variant G/A,C snp 5
rs267607149 0.846 0.107 12 109784385 missense variant C/T snp 5
rs77975504 0.878 0.250 12 109792695 missense variant C/T snp 5
rs886044555 0.923 0.071 12 47985772 missense variant C/T snp 4
rs369614706 0.878 0.107 11 103120705 missense variant C/T snp 2.4E-05 4
rs387906902 0.878 0.071 12 109793560 missense variant G/C,T snp 4.0E-06 4
rs74315304 0.923 0.107 1 150799228 missense variant G/A,T snp 4.0E-06; 4.0E-06 3
rs121912632 0.878 0.071 12 109792407 missense variant C/T snp 3
rs267607148 0.923 0.071 12 109800639 missense variant C/T snp 3
rs387906906 0.923 0.107 12 109786827 missense variant G/A snp 3
rs387906907 0.923 0.107 12 109800645 missense variant T/C snp 3
rs397514474 0.923 0.107 12 109814565 missense variant C/A snp 3
rs1057516230 0.923 0.071 1 21554127 frameshift variant TAACT/T in-del 2
rs1057518967 1.000 0.036 7 94423102 missense variant G/A snp 2
rs116571438 0.923 0.071 12 109788483 stop gained G/A,T snp 8.0E-06 2