Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs77375493 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 187
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144
rs2736100 0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs104894230 0.564 0.600 11 534288 missense variant C/A;G;T snv 73
rs121913237 0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 50
rs727503094 0.633 0.440 11 534287 missense variant GC/AG;AT;TA;TT mnv 41
rs121913615
MPL
0.683 0.240 1 43349338 missense variant G/C;T snv 8.0E-06 25
rs121918464 0.708 0.440 12 112450406 missense variant G/A;C snv 25
rs121913502 0.708 0.320 15 90088702 missense variant C/A;T snv 3.2E-05 19
rs562015640 0.742 0.360 10 87960957 stop gained A/G;T snv 1.2E-05 16
rs16754
WT1
0.732 0.240 11 32396399 synonymous variant T/C snv 0.24; 4.0E-06 0.17 15
rs121918462 0.742 0.320 12 112450398 missense variant C/T snv 13
rs796065343 0.776 0.080 1 36467833 missense variant G/A snv 12
rs201478192 0.790 0.200 2 8731667 missense variant C/A snv 2.4E-04 2.6E-04 12
rs9376092 0.851 0.120 6 135106006 upstream gene variant C/A snv 0.24 10
rs12343867 0.790 0.200 9 5074189 intron variant T/C snv 0.25 9
rs104894365 0.827 0.320 12 25245345 missense variant C/T snv 9
rs121913616
MPL
0.790 0.120 1 43349337 missense variant TG/AA mnv 8
rs397507510 0.776 0.280 12 112450361 missense variant G/A;C;T snv 8
rs121913614
MPL
0.790 0.120 1 43349308 missense variant G/A snv 7
rs1057519819 0.851 0.240 15 66436750 missense variant T/C snv 6
rs1057520016 0.851 0.080 9 5089726 missense variant C/A;T snv 5
rs12342421 0.851 0.080 9 5065750 intron variant G/C snv 0.23 5
rs556915505 0.851 0.080 3 169143780 missense variant T/C snv 4.0E-06 7.0E-06 5