Disease: Childhood Acute Lymphoblastic Leukemia
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6461639
RAPGEF5
0.882 0.120 7 22147337 intron variant T/A;C snv 3
rs6535455
HPSE
0.851 0.160 4 83310951 intron variant T/A;C snv 4
rs7039798
FPGS
0.882 0.120 9 127794947 intron variant G/A;C snv 3
rs7088318
PIP4K2A
0.851 0.120 10 22564019 intron variant C/A snv 0.55 4
rs7089424
ARID5B
0.752 0.200 10 61992400 intron variant T/G snv 0.32 10
rs7286979
EP300
0.882 0.120 22 41102623 intron variant G/A snv 0.26 3
rs755622
MIF-AS1 ; MIF
0.611 0.720 22 23894205 intron variant G/C snv 0.26 44
rs7809758
DDC ; FIGNL1
0.882 0.120 7 50505635 intron variant A/G snv 0.36 3
rs880028
FIGNL1 ; DDC
0.882 0.120 7 50502438 intron variant A/G snv 0.21 3
rs924607
LOC105374608 ; LOC100996325
0.851 0.120 5 609978 intron variant C/T snv 0.32 7
rs17007695 0.851 0.120 4 141788570 intergenic variant T/C snv 7.7E-02 4
rs4748793 0.851 0.120 10 22194082 intergenic variant A/G snv 0.18 4
rs35201683
HFE
0.732 0.360 6 26094205 stop gained C/A;T snv 1.4E-03 12
rs368005287
CYP3A4
0.882 0.120 7 99762071 stop gained C/T snv 1.2E-05 7.0E-06 3
rs755001634
FOLH1
0.763 0.280 11 49154384 stop gained G/A snv 1.2E-05 13
rs780246573
HFE ; LOC108783645
0.732 0.360 6 26092860 stop gained C/G;T snv 4.0E-06; 8.0E-06 12
rs797045145
HFE ; LOC108783645
0.807 0.240 6 26091479 stop gained G/A snv 6
rs80338880
TFR2
0.732 0.360 7 100633100 stop gained G/C snv 7.0E-06 12
rs1039659576
MTR
0.689 0.520 1 236803473 missense variant A/G snv 21
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs104893636
HOXD4 ; HOXD3
0.882 0.120 2 176151875 missense variant A/C;T snv 5.2E-06; 7.9E-04 3
rs1057519743
CRLF2
0.827 0.120 Y 1196852 missense variant A/C snv 6
rs1057519866
NT5C2
0.851 0.120 10 103093198 missense variant C/T snv 5
rs10828317
PIP4K2A
0.776 0.280 10 22550699 missense variant T/C snv 9
rs11099592
HPSE
0.851 0.160 4 83309466 missense variant T/C snv 0.78 0.80 5