Disease: Leukemia, Myelocytic, Acute
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs77375493
INSL6 ; JAK2
0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 187
rs13181
KLC3 ; ERCC2
0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs2032582
ABCB1
0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs11554290
NRAS
0.583 0.600 1 114713908 missense variant T/A;C;G snv 59
rs4553808
CTLA4
0.672 0.320 2 203866282 upstream gene variant A/G;T snv 0.16 28
rs16754
WT1
0.732 0.240 11 32396399 synonymous variant T/C snv 0.24; 4.0E-06 0.17 15
rs2239633
CEBPE
0.742 0.240 14 23119848 upstream gene variant G/A snv 0.38 12
rs10821936
ARID5B
0.742 0.200 10 61963818 intron variant C/T snv 0.69 11
rs7089424
ARID5B
0.752 0.200 10 61992400 intron variant T/G snv 0.32 10
rs1057519753
JAK1
0.763 0.120 1 64846664 missense variant C/A snv 9
rs11978267
IKZF1
0.763 0.240 7 50398606 intron variant A/G snv 0.25 9
rs10994982
ARID5B
0.790 0.120 10 61950345 intron variant A/G snv 0.49 7
rs121913488
FLT3
0.807 0.120 13 28018505 missense variant C/A;G;T snv 7
rs7073837
ARID5B
0.851 0.120 10 61940136 intron variant A/C snv 0.58 0.64 4
rs121909646
FLT3
0.882 0.120 13 28018504 missense variant T/A;G snv 3
rs121913232
FLT3
0.925 0.120 13 28018500 missense variant G/C snv 2
rs121913487
FLT3
0.925 0.120 13 28018503 missense variant A/C;T snv 2
rs2242041
FIGNL1 ; DDC
0.925 0.120 7 50461751 intron variant C/G snv 7.7E-02 2