Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1057519695 0.641 0.520 1 114713907 missense variant TT/CA;CC mnv 35
rs1057519753 0.763 0.120 1 64846664 missense variant C/A snv 9
rs1057519773 0.851 0.160 9 130872901 missense variant T/A;C;G snv 4
rs1057519834 0.658 0.480 1 114713908 missense variant TG/CT mnv 31
rs10740055 0.790 0.240 10 61958720 intron variant C/A snv 0.49 7
rs10821936 0.742 0.200 10 61963818 intron variant C/T snv 0.69 11
rs10994982 0.790 0.120 10 61950345 intron variant A/G snv 0.49 7
rs1142345 0.776 0.280 6 18130687 missense variant T/C;G snv 3.7E-02 9
rs11554290 0.583 0.600 1 114713908 missense variant T/A;C;G snv 59
rs116855232 0.742 0.400 13 48045719 missense variant C/T snv 2.8E-02 1.1E-02 12
rs11978267 0.763 0.240 7 50398606 intron variant A/G snv 0.25 9
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs121909646 0.882 0.120 13 28018504 missense variant T/A;G snv 3
rs121913448 0.827 0.120 9 130862976 missense variant G/A snv 5
rs121913451 0.851 0.160 9 130872903 missense variant C/A;G snv 4
rs121913459 0.672 0.160 9 130872896 missense variant C/T snv 25
rs121913488 0.807 0.120 13 28018505 missense variant C/A;G;T snv 7
rs121913615
MPL
0.683 0.240 1 43349338 missense variant G/C;T snv 8.0E-06 25
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs1339159756 0.925 0.120 9 5078395 missense variant C/G snv 2
rs147390019 0.925 0.120 13 48045720 missense variant G/A snv 2.6E-03 2.2E-03 2
rs153109 0.623 0.600 16 28507775 intron variant T/C snv 0.43 37
rs16754
WT1
0.732 0.240 11 32396399 synonymous variant T/C snv 0.24; 4.0E-06 0.17 15
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188