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
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs17576
MMP9
0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 73
rs318699
RGL3
0.882 0.080 19 11390564 intron variant A/G snv 0.73 3
rs4073
CXCL8
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 64
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
rs1057519753
JAK1
0.763 0.120 1 64846664 missense variant C/A snv 9
rs1200469268
ABCA1
0.925 0.080 9 104830968 missense variant C/A snv 7.0E-06 2
rs7046736
JAK2 ; INSL6
0.925 0.080 9 5015732 intron variant C/A snv 0.39 2
rs1188383936
F2
0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 102
rs12979860
IFNL4
0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs780178275
VHL
0.851 0.200 3 10146586 missense variant C/T snv 8.0E-06 7
rs773475680
ABL1
1.000 0.080 9 130884139 missense variant C/T snv 4.0E-06 1
rs361525
TNF
0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 62
rs775387828
NFE2
0.851 0.200 12 54293083 missense variant G/A snv 2.2E-05 7.0E-06 7
rs10974947
INSL6 ; JAK2
0.882 0.080 9 5072846 intron variant G/A snv 0.23 3
rs1253570532
RUNX1
0.925 0.080 21 34792289 missense variant G/A snv 7.0E-06 2
rs754190776
HBG2
0.925 0.080 11 5253350 missense variant G/A snv 8.0E-06 2
rs772889171
RUNX1
0.925 0.080 21 34834487 missense variant G/A snv 4.0E-06 2
rs267606870
IDH2
0.763 0.280 15 90088703 missense variant G/A;C snv 11
rs121913499
IDH1
0.605 0.520 2 208248389 missense variant G/A;C;T snv 51
rs77375493
INSL6 ; JAK2
0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 187