Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4246215
FADS2 ; FEN1
0.677 0.320 11 61796827 3 prime UTR variant G/C;T snv 29
rs1801394
FASTKD3 ; MTRR
0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs61753793
FBXO11 ; MSH6
0.851 0.120 2 47799002 missense variant T/C snv 3.6E-05 5.6E-05 4
rs121909629
FGFR1
0.882 0.200 8 38415905 missense variant C/T snv 3
rs1444068378
FHL2
1.000 0.040 2 105363404 missense variant G/A snv 4.0E-06 1
rs121913488
FLT3
0.807 0.120 13 28018505 missense variant C/A;G;T snv 7
rs1057519766
FLT3
0.851 0.080 13 28028203 missense variant G/C;T snv 5
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
rs11545078
GGH
0.807 0.200 8 63026205 missense variant G/A snv 8.8E-02 7.8E-02 6
rs1275561861
HLA-A
0.672 0.360 6 29944350 missense variant G/A snv 23
rs138213197
HOXB13
0.701 0.240 17 48728343 missense variant C/T snv 1.8E-03 1.6E-03 24
rs104894230
HRAS ; LRRC56
0.564 0.600 11 534288 missense variant C/A;G;T snv 73
rs121913502
IDH2
0.708 0.320 15 90088702 missense variant C/A;T snv 3.2E-05 19
rs6964823
IKZF1
0.925 0.040 7 50392398 intron variant G/A snv 0.45 3
rs774164690
IKZF1
1.000 0.040 7 50400428 missense variant C/T snv 1
rs2243250
IL4
0.570 0.760 5 132673462 upstream gene variant C/T snv 0.35 61
rs2070874
IL4
0.672 0.560 5 132674018 5 prime UTR variant C/T snv 0.28 0.28 27
rs77375493
INSL6 ; JAK2
0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 187
rs10065633
IRF1-AS1
1.000 0.040 5 132481024 intron variant T/C snv 0.38 1
rs1057519753
JAK1
0.763 0.120 1 64846664 missense variant C/A snv 9
rs869312953
JAK1
0.851 0.120 1 64846735 missense variant G/T snv 5
rs923941004
JAK2 ; INSL6
1.000 0.040 9 5078334 missense variant T/C snv 1
rs121913682
KIT
0.605 0.400 4 54733167 missense variant A/G;T snv 52
rs121913507
KIT
0.614 0.400 4 54733155 missense variant A/T snv 49