Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104894230
HRAS ; LRRC56
0.564 0.600 11 534288 missense variant C/A;G;T snv 73
rs104894365
KRAS
0.827 0.320 12 25245345 missense variant C/T snv 9
rs1057519721
INSL6 ; JAK2
0.882 0.120 9 5078360 missense variant A/G snv 4
rs1057519752
MPL
1.000 0.080 1 43349307 missense variant A/C;G;T snv 1
rs1057519819
MAP2K1
0.851 0.240 15 66436750 missense variant T/C snv 6
rs1057520016
JAK2 ; INSL6
0.851 0.080 9 5089726 missense variant C/A;T snv 5
rs10974944
JAK2 ; INSL6
0.882 0.160 9 5070831 intron variant C/G snv 0.25 4
rs1200469268
ABCA1
0.925 0.080 9 104830968 missense variant C/A snv 7.0E-06 2
rs121912473
JAK2 ; INSL6
0.925 0.080 9 5070026 missense variant AA/TT mnv 3
rs121913237
NRAS
0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 50
rs121913502
IDH2
0.708 0.320 15 90088702 missense variant C/A;T snv 3.2E-05 19
rs121913504
JAK3
0.882 0.080 19 17837200 missense variant G/A snv 3
rs121913520
KIT
1.000 0.080 4 54727443 missense variant G/A snv 4
rs121913529
KRAS
0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144
rs121913614
MPL
0.790 0.120 1 43349308 missense variant G/A snv 7
rs121913615
MPL
0.683 0.240 1 43349338 missense variant G/C;T snv 8.0E-06 25
rs121913616
MPL
0.790 0.120 1 43349337 missense variant TG/AA mnv 8
rs121918462
PTPN11
0.742 0.320 12 112450398 missense variant C/T snv 13
rs121918464
PTPN11
0.708 0.440 12 112450406 missense variant G/A;C snv 25
rs12339666
INSL6 ; JAK2
0.925 0.080 9 5063296 intron variant G/T snv 0.34 3
rs12340895
INSL6 ; JAK2
1.000 0.080 9 5076691 intron variant C/A;G snv 1
rs12342421
JAK2 ; INSL6
0.851 0.080 9 5065750 intron variant G/C snv 0.23 5
rs12343867
INSL6 ; JAK2
0.790 0.200 9 5074189 intron variant T/C snv 0.25 9
rs1259653415
TFRC
1.000 0.080 3 196071416 missense variant T/C snv 7.0E-06 3
rs1441084781
TLR4
1.000 0.080 9 117712543 missense variant G/A;T snv 4.0E-06 1