Disease: Leukemia, Myelocytic, Acute
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12147254
TRAF3
0.851 0.240 14 102799329 intron variant G/A snv 0.23 4
rs121917759
HRAS ; LRRC56
0.790 0.480 11 533466 missense variant G/A snv 8
rs104894231
LRRC56 ; HRAS
0.776 0.360 11 533467 missense variant C/G;T snv 9
rs267606870
IDH2
0.763 0.280 15 90088703 missense variant G/A;C snv 11
rs1057519978
TP53
0.763 0.360 17 7675191 missense variant A/C;G;T snv 12
rs1057519977
TP53
0.763 0.360 17 7675189 missense variant G/C snv 13
rs587781288
TP53
0.732 0.440 17 7675190 missense variant C/A;T snv 16
rs121434595
NRAS
0.708 0.320 1 114716124 missense variant C/A;G;T snv 19
rs121913502
IDH2
0.708 0.320 15 90088702 missense variant C/A;T snv 3.2E-05 19
rs942158624
TP53
0.724 0.320 17 7674948 missense variant T/A snv 19
rs121913240
KRAS
0.672 0.440 12 25227342 missense variant T/A;C;G snv 24
rs121913250
NRAS
0.683 0.440 1 114716127 missense variant C/A;G;T snv 25
rs121918464
PTPN11
0.708 0.440 12 112450406 missense variant G/A;C snv 25
rs121434596
NRAS
0.677 0.440 1 114716123 missense variant C/A;G;T snv 4.0E-06; 4.0E-06 26
rs121913255
NRAS
0.667 0.400 1 114713907 missense variant T/A;G snv 26
rs17851045
KRAS
0.672 0.400 12 25227341 missense variant T/A;G snv 4.0E-06 27
rs28933406
LRRC56 ; HRAS
0.667 0.480 11 533875 missense variant G/C;T snv 27
rs104894226
LRRC56 ; HRAS
0.658 0.560 11 534285 missense variant C/A;G;T snv 29
rs760043106
TP53
0.645 0.440 17 7674947 missense variant A/C;G;T snv 32
rs1884444
IL23R ; C1orf141
0.637 0.600 1 67168129 missense variant G/T snv 0.52 0.51 34
rs121913233
HRAS ; LRRC56
0.627 0.520 11 533874 missense variant T/A;C;G snv 37
rs121913343
TP53
0.611 0.520 17 7673803 missense variant G/A;C;T snv 1.2E-05 44
rs104894228
LRRC56 ; HRAS
0.605 0.560 11 534286 missense variant C/A;G;T snv 48
rs121913237
NRAS
0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 50
rs121913499
IDH1
0.605 0.520 2 208248389 missense variant G/A;C;T snv 51