Source: UNIPROT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1169288572
SETD2
1.000 0.040 3 47122237 missense variant C/T snv 8.0E-06 7.0E-06 1
rs1466524306
UBAC2 ; GPR183
1.000 0.040 13 99295133 missense variant G/A snv 4.0E-06 1
rs267606708
CBL
0.925 0.040 11 119278541 missense variant G/A snv 4.0E-06 2.1E-05 1
rs28931590
CEBPA ; CEBPA-DT
1.000 0.040 19 33302164 missense variant T/A snv 1
rs754921650
SETD2
1.000 0.040 3 47120446 missense variant T/C snv 1.2E-05 2.1E-05 1
rs387906631
GATA2
0.882 0.080 3 128481901 missense variant G/A snv 2
rs569067880
TET2-AS1 ; TET2
0.925 0.080 4 105234864 missense variant G/A;C snv 4.0E-06; 4.0E-06 2
rs1057519709
KIT
0.925 0.080 4 54733154 missense variant GA/AT mnv 1
rs121912472
INSL6 ; JAK2
0.925 0.080 9 5073742 missense variant G/C snv 1
rs137854451
ELANE
0.925 0.080 19 856000 missense variant G/A snv 1
rs387906629
GATA2
0.925 0.080 3 128481270 missense variant G/A snv 1
rs57246956
ELANE
0.882 0.080 19 855649 missense variant G/A;T snv 1
rs869312828
DDX41 ; DOK3
0.807 0.080 5 177512369 missense variant C/T snv 1
rs121913487
FLT3
0.925 0.120 13 28018503 missense variant A/C;T snv 2
rs1057519906
IDH2
0.882 0.120 15 90088607 missense variant T/A;C snv 1
rs121909646
FLT3
0.882 0.120 13 28018504 missense variant T/A;G snv 1
rs121913232
FLT3
0.925 0.120 13 28018500 missense variant G/C snv 1
rs121913488
FLT3
0.807 0.120 13 28018505 missense variant C/A;G;T snv 1
rs387907097
TGM6
0.925 0.120 20 2417445 missense variant T/G snv 1.5E-04 5.6E-05 1
rs74315450
RUNX1
0.851 0.120 21 34859485 missense variant C/T snv 1
rs371246226
U2AF1
0.827 0.160 21 43094667 missense variant T/C;G snv 2.4E-05; 2.4E-05 1
rs121913503
IDH2
0.689 0.200 15 90088606 missense variant C/A;T snv 1
rs483352695
TP53
0.882 0.200 17 7674227 missense variant T/A;C;G snv 1
rs587782529
TP53
0.851 0.200 17 7670700 missense variant G/A;C snv 1
rs111033563
LOC108783645 ; HFE
0.776 0.240 6 26092916 missense variant A/C snv 4.0E-06 1