Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs998297769 X 151962587 stop gained G/T snv 1.1E-05 2.8E-05 1
rs984649575 12 122377616 stop gained G/A snv 2.1E-05 1
rs886043613 0.925 0.080 4 1801519 missense variant C/T snv 4
rs886041093 0.827 0.280 9 137815998 missense variant G/A snv 7
rs886039900 0.925 0.320 1 27549887 frameshift variant C/- delins 8
rs879253753 0.851 0.280 16 89280526 frameshift variant -/T delins 19
rs875989883 0.851 0.280 X 22219070 missense variant G/A;C snv 9
rs875989777 0.851 0.320 20 45894704 frameshift variant AT/- delins 9
rs869312707 0.925 0.160 12 115963422 missense variant G/A snv 4
rs869312687 0.925 0.080 1 155910695 missense variant T/G snv 8
rs869025191 0.827 0.160 1 155904739 missense variant C/A;G;T snv 9
rs867410737 0.708 0.440 19 1242559 missense variant C/T snv 6.7E-06 42
rs864309521 1.000 0.200 6 43043631 splice acceptor variant C/G snv 2
rs80338903 0.701 0.360 1 216247095 frameshift variant C/- del 7.6E-04 5.4E-04 25
rs80338796 0.667 0.480 3 12604200 missense variant G/A;C snv 4.0E-06 35
rs797045283 0.827 0.320 6 157207109 stop gained C/T snv 11
rs797044526 0.925 21 37490393 missense variant C/T snv 7
rs797044525 0.925 21 37490244 missense variant T/G snv 9
rs797044524 0.925 21 37486513 missense variant A/T snv 9
rs797044523 0.882 21 37480756 frameshift variant -/A delins 9
rs797044522 0.925 21 37496119 frameshift variant AGAT/- delins 9
rs797044521 0.925 21 37480768 frameshift variant A/- delins 8
rs797044520 0.925 21 37505442 stop gained C/T snv 6
rs797044519 0.925 21 37478285 stop gained C/A;G;T snv 9
rs796052686 0.776 0.280 7 66638394 missense variant G/A snv 1.2E-05 22