Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12672038
CAV1
0.925 0.080 7 116547052 intron variant G/A snv 7.6E-02 4
rs3757733
CAV1
1.000 0.040 7 116553675 intron variant T/A snv 0.26 4
rs754944509
CNTNAP1
0.851 0.080 17 42690793 missense variant C/T snv 4.4E-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
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
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
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
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
rs74315450
RUNX1
0.851 0.120 21 34859485 missense variant C/T snv 5
rs1408538785
DNAH8
0.827 0.080 6 38761760 missense variant A/G snv 7.0E-06 6
rs387906553
ELANE
0.827 0.120 19 853022 missense variant G/A;C snv 1.2E-05 6
rs2413739
PACSIN2
0.827 0.120 22 43001030 intron variant C/T snv 0.43 6
rs1360131632
STAT5A
0.827 0.080 17 42301316 missense variant C/T snv 4.0E-06 6
rs10740055
ARID5B
0.790 0.240 10 61958720 intron variant C/A snv 0.49 7
rs869312828
DDX41 ; DOK3
0.807 0.080 5 177512369 missense variant C/T snv 7
rs121913488
FLT3
0.807 0.120 13 28018505 missense variant C/A;G;T snv 7
rs762613037
SLC19A1 ; COL18A1
0.790 0.160 21 45512196 missense variant A/G snv 2.1E-05 7.0E-06 7
rs748843032
MTTP
0.807 0.160 4 99594840 missense variant T/C snv 4.0E-06 8