Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs766274360
PRSS27
0.882 0.040 16 2713697 missense variant G/T snv 1.2E-05 3
rs139834892
XRCC1
0.882 0.040 19 43553481 missense variant C/T snv 6.4E-05 1.1E-04 3
rs974120 0.851 0.200 8 2789080 intron variant T/C;G snv 4
rs121913452
ABL1
0.851 0.080 9 130873027 missense variant T/A;C;G snv 4
rs1188975135
APOBEC3C ; APOBEC3F
0.882 0.040 22 39017772 missense variant T/C snv 4.0E-06 4
rs397507476
BRAF
0.882 0.200 7 140778011 missense variant T/A;G snv 4
rs754944509
CNTNAP1
0.851 0.080 17 42690793 missense variant C/T snv 4.4E-05 4
rs61753793
FBXO11 ; MSH6
0.851 0.120 2 47799002 missense variant T/C snv 3.6E-05 5.6E-05 4
rs35602083
FLT3
0.851 0.040 13 28049450 missense variant C/T snv 1.7E-02 1.6E-02 4
rs753000469
FLVCR1-DT ; FLVCR1
0.851 0.200 1 212859113 missense variant C/T snv 4.0E-06 4
rs104894421
LIG4
0.882 0.200 13 108210436 missense variant C/A;T snv 1.2E-05 4
rs138817062
PML
0.882 0.040 15 74044940 missense variant C/T snv 4.0E-05 7.0E-06 4
rs1360698171
RNASEL
0.851 0.080 1 182584103 missense variant T/C snv 4
rs11079041
STAT5B
0.882 0.040 17 42262061 intron variant T/A;C snv 0.36 4
rs10251201
UMAD1
0.851 0.160 7 7932654 intron variant T/A;C snv 4
rs121913448
ABL1
0.827 0.120 9 130862976 missense variant G/A snv 5
rs121913461
ABL1
0.851 0.120 9 130862970 missense variant T/C snv 5
rs780634396
BCL2
0.882 0.120 18 63318618 missense variant T/C snv 4.0E-06 5
rs387906666
CBL
0.827 0.080 11 119278182 missense variant A/C;G snv 5
rs1057519766
FLT3
0.851 0.080 13 28028203 missense variant G/C;T snv 5
rs869312953
JAK1
0.851 0.120 1 64846735 missense variant G/T snv 5
rs556915505
MECOM
0.851 0.080 3 169143780 missense variant T/C snv 4.0E-06 7.0E-06 5
rs1057519866
NT5C2
0.851 0.120 10 103093198 missense variant C/T snv 5
rs74315450
RUNX1
0.851 0.120 21 34859485 missense variant C/T snv 5
rs387906517
ABL1
0.827 0.120 9 130862919 missense variant G/A snv 6