Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs61752717 0.583 0.840 16 3243407 missense variant T/A;C snv 2.8E-04 72
rs153109 0.623 0.600 16 28507775 intron variant T/C snv 0.43 37
rs121913355 0.641 0.520 7 140781602 missense variant C/A;G;T snv 4.0E-06 42
rs397507520 0.658 0.520 12 112453279 missense variant G/C;T snv 39
rs121918459 0.662 0.440 12 112450368 missense variant A/G snv 1.2E-05 7.0E-06 47
rs1057519925 0.683 0.560 3 179210291 missense variant G/A;C snv 25
rs1057519389 0.695 0.400 10 129957324 missense variant C/A;G;T snv 46
rs17855750 0.695 0.480 16 28503907 missense variant A/C;T snv 6.4E-02; 4.0E-06 21
rs765379963 0.701 0.520 1 165743172 stop gained G/A snv 1.2E-05 2.1E-05 19
rs397507545 0.708 0.560 12 112489083 missense variant G/A;C snv 4.0E-06 20
rs180177135 0.716 0.520 16 23607891 frameshift variant T/- del 2.1E-05 27
rs1060499548 0.724 0.440 9 130872961 missense variant G/A snv 27
rs875989800 0.732 0.480 22 23833670 inframe deletion AGA/- delins 33
rs587784105 0.732 0.440 5 177235863 stop gained G/A snv 19
rs1566823361 0.742 0.440 13 101726732 frameshift variant -/G delins 18
rs12508721 0.742 0.360 4 122623509 intron variant C/T snv 0.24 11
rs1556425596 0.752 0.240 21 45989967 intron variant C/T snv 37
rs387906692 0.752 0.480 17 68530405 stop gained C/T snv 11
rs907715 0.752 0.520 4 122613898 intron variant C/T snv 0.35 11
rs397517154 0.763 0.280 2 39022773 missense variant C/A;G;T snv 4.0E-06 16
rs7977932 0.763 0.320 12 122172836 intron variant C/G;T snv 10
rs4758680 0.763 0.320 12 122170805 intron variant T/A;G snv 9
rs138632121 0.776 0.400 16 3026140 missense variant T/A snv 1.7E-04 2.0E-04 13
rs1562134961 0.776 0.320 6 78969879 frameshift variant A/- delins 13
rs200426926 0.776 0.400 16 3027379 missense variant G/A;T snv 1.8E-04; 4.0E-06 13