Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs869312828
DDX41 ; DOK3
0.807 0.080 5 177512369 missense variant C/T snv 7
rs1360131632
STAT5A
0.827 0.080 17 42301316 missense variant C/T snv 4.0E-06 6
rs1408538785
DNAH8
0.827 0.080 6 38761760 missense variant A/G snv 7.0E-06 6
rs1057519766
FLT3
0.851 0.080 13 28028203 missense variant G/C;T 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
rs121913452
ABL1
0.851 0.080 9 130873027 missense variant T/A;C;G snv 4
rs12672038
CAV1
0.925 0.080 7 116547052 intron variant G/A snv 7.6E-02 4
rs1360698171
RNASEL
0.851 0.080 1 182584103 missense variant T/C snv 4
rs754944509
CNTNAP1
0.851 0.080 17 42690793 missense variant C/T snv 4.4E-05 4
rs10405859
PPP1R37 ; MARK4
0.882 0.080 19 45099523 intron variant T/C snv 0.48 3
rs9318227
KLF12
0.882 0.080 13 73926833 intron variant T/A;C snv 3
rs121913521
KIT
0.790 0.120 4 54727447 missense variant T/A;C;G snv 12
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
rs121913488
FLT3
0.807 0.120 13 28018505 missense variant C/A;G;T snv 7
rs2413739
PACSIN2
0.827 0.120 22 43001030 intron variant C/T snv 0.43 6
rs387906553
ELANE
0.827 0.120 19 853022 missense variant G/A;C snv 1.2E-05 6
rs121913461
ABL1
0.851 0.120 9 130862970 missense variant T/C snv 5
rs74315450
RUNX1
0.851 0.120 21 34859485 missense variant C/T snv 5
rs780634396
BCL2
0.882 0.120 18 63318618 missense variant T/C snv 4.0E-06 5
rs869312953
JAK1
0.851 0.120 1 64846735 missense variant G/T snv 5
rs3794845
MBP
0.882 0.120 18 77002561 intron variant G/C snv 0.12 3
rs703817
STAT6
0.925 0.120 12 57096045 3 prime UTR variant C/T snv 0.39 2
rs121913459
ABL1
0.672 0.160 9 130872896 missense variant C/T snv 25