Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs562533120
HBS1L
0.882 0.080 6 134966397 missense variant A/C snv 8.0E-06 3
rs1057519752
MPL
1.000 0.080 1 43349307 missense variant A/C;G;T snv 1
rs1057519721
INSL6 ; JAK2
0.882 0.120 9 5078360 missense variant A/G snv 4
rs562015640
PTEN
0.742 0.360 10 87960957 stop gained A/G;T snv 1.2E-05 16
rs59384377
INSL6 ; JAK2
1.000 0.080 9 5005034 intron variant A/T snv 0.26 1
rs121912473
JAK2 ; INSL6
0.925 0.080 9 5070026 missense variant AA/TT mnv 3
rs2736100
TERT
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs201478192
KIDINS220
0.790 0.200 2 8731667 missense variant C/A snv 2.4E-04 2.6E-04 12
rs9376092
LOC105378010
0.851 0.120 6 135106006 upstream gene variant C/A snv 0.24 10
rs778767225
MOK
0.851 0.200 14 102231805 missense variant C/A snv 2.4E-05 7.0E-06 4
rs1200469268
ABCA1
0.925 0.080 9 104830968 missense variant C/A snv 7.0E-06 2
rs12340895
INSL6 ; JAK2
1.000 0.080 9 5076691 intron variant C/A;G snv 1
rs121913529
KRAS
0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144
rs104894230
HRAS ; LRRC56
0.564 0.600 11 534288 missense variant C/A;G;T snv 73
rs121913237
NRAS
0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 50
rs4858647 0.925 0.080 3 24749884 intron variant C/A;G;T snv 2
rs121913502
IDH2
0.708 0.320 15 90088702 missense variant C/A;T snv 3.2E-05 19
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
rs121918462
PTPN11
0.742 0.320 12 112450398 missense variant C/T snv 13
rs104894365
KRAS
0.827 0.320 12 25245345 missense variant C/T snv 9
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs796065343
CSF3R
0.776 0.080 1 36467833 missense variant G/A snv 12
rs121913614
MPL
0.790 0.120 1 43349308 missense variant G/A snv 7
rs121913520
KIT
1.000 0.080 4 54727443 missense variant G/A snv 4