Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2075685
TMEM167A ; XRCC4
0.724 0.320 5 83076846 intron variant G/A;T snv 14
rs387906659
AKT2
0.742 0.280 19 40257052 stop gained C/A;T snv 14
rs2075686
TMEM167A ; XRCC4
0.742 0.240 5 83076927 intron variant C/T snv 1.7E-02 13
rs121913514
KIT
0.763 0.240 4 54733174 missense variant T/A;G snv 12
rs121913521
KIT
0.790 0.120 4 54727447 missense variant T/A;C;G snv 12
rs796065343
CSF3R
0.776 0.080 1 36467833 missense variant G/A snv 12
rs10821936
ARID5B
0.742 0.200 10 61963818 intron variant C/T snv 0.69 11
rs1470755915
RUNX1T1
0.776 0.240 8 92005229 missense variant C/A snv 7.0E-06 10
rs1057519753
JAK1
0.763 0.120 1 64846664 missense variant C/A snv 9
rs2293157
STAT5A
0.763 0.120 17 42300657 intron variant C/A;T snv 9
rs7727691
XRCC4 ; TMEM167A
0.763 0.200 5 83075876 intron variant C/T snv 0.32 9
rs1482518887
RUNX1
0.790 0.040 21 34887018 missense variant C/T snv 7.0E-06 8
rs10740055
ARID5B
0.790 0.240 10 61958720 intron variant C/A snv 0.49 7
rs121913488
FLT3
0.807 0.120 13 28018505 missense variant C/A;G;T snv 7
rs869312828
DDX41 ; DOK3
0.807 0.080 5 177512369 missense variant C/T snv 7
rs1408538785
DNAH8
0.827 0.080 6 38761760 missense variant A/G snv 7.0E-06 6
rs2413739
PACSIN2
0.827 0.120 22 43001030 intron variant C/T snv 0.43 6
rs1057519766
FLT3
0.851 0.080 13 28028203 missense variant G/C;T snv 5
rs121913461
ABL1
0.851 0.120 9 130862970 missense variant T/C snv 5
rs3807992
CAV1
0.925 0.080 7 116557191 intron variant G/A snv 0.28 5
rs387906666
CBL
0.827 0.080 11 119278182 missense variant A/C;G snv 5
rs74315450
RUNX1
0.851 0.120 21 34859485 missense variant C/T snv 5
rs869312953
JAK1
0.851 0.120 1 64846735 missense variant G/T snv 5
rs10251201
UMAD1
0.851 0.160 7 7932654 intron variant T/A;C snv 4
rs11079041
STAT5B
0.882 0.040 17 42262061 intron variant T/A;C snv 0.36 4