Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1408538785
DNAH8
0.827 0.080 6 38761760 missense variant A/G snv 7.0E-06 6
rs1265794840
ERCC2
0.851 0.160 19 45365131 missense variant C/T snv 7.0E-06 6
rs387906631
GATA2
0.882 0.080 3 128481901 missense variant G/A snv 6
rs1464681682
LOC102724701 ; U2AF1L5 ; LOC102724843
0.882 0.160 21 6486334 missense variant T/C;G snv 6
rs397507548
PTPN11
0.851 0.160 12 112489093 missense variant A/C snv 6
rs2454206
TET2-AS1 ; TET2
0.851 0.160 4 105275794 missense variant A/G;T snv 0.30; 6.4E-06 6
rs387906717
WAS
0.827 0.120 X 48688403 missense variant T/C snv 6
rs869312828
DDX41 ; DOK3
0.807 0.080 5 177512369 missense variant C/T snv 7
rs377577594
DNMT3A
0.827 0.240 2 25234374 missense variant G/A;C;T snv 1.2E-04; 8.0E-06 7
rs121913488
FLT3
0.807 0.120 13 28018505 missense variant C/A;G;T snv 7
rs1057519960
SF3B2
0.827 0.280 11 66063413 missense variant A/G snv 7
rs2230641
CCNH
0.807 0.240 5 87399457 missense variant A/G;T snv 0.18 0.17 8
rs371246226
U2AF1
0.827 0.160 21 43094667 missense variant T/C;G snv 2.4E-05; 2.4E-05 8
rs2308327
MGMT
0.790 0.280 10 129766906 missense variant A/G snv 9.4E-02 8.7E-02 10
rs1470755915
RUNX1T1
0.776 0.240 8 92005229 missense variant C/A snv 7.0E-06 10
rs927698341
RUNX1T1
0.776 0.240 8 92005280 synonymous variant C/A snv 4.0E-06 2.8E-05 10
rs267606870
IDH2
0.763 0.280 15 90088703 missense variant G/A;C snv 11
rs1805388
LIG4
0.790 0.120 13 108211243 missense variant G/A snv 0.18 0.16 11
rs8179090
TIMP2
0.752 0.280 17 78925807 upstream gene variant C/G snv 1.6E-02 12
rs2228526
ERCC6
0.752 0.200 10 49470671 missense variant T/C snv 0.22 0.19 13
rs559063155
SF3B1
0.732 0.280 2 197402110 stop gained T/A;C;G snv 9.0E-05 14
rs745564626
XRCC3 ; KLC1
0.752 0.280 14 103699003 missense variant C/G;T snv 4.3E-05 14
rs147001633
DNMT3A
0.776 0.240 2 25234373 missense variant C/A;G;T snv 4.0E-06; 4.0E-06; 2.2E-04 15
rs1617640
EPO
0.742 0.520 7 100719675 upstream gene variant C/A;G;T snv 15
rs755174338
ERCC2
0.732 0.360 19 45364096 missense variant C/T snv 2.6E-05 1.4E-05 15