Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs12979860
IFNL4
0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs2736100
TERT
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs4073
CXCL8
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 64
rs361525
TNF
0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 62
rs121913499
IDH1
0.605 0.520 2 208248389 missense variant G/A;C;T snv 51
rs267606870
IDH2
0.763 0.280 15 90088703 missense variant G/A;C snv 11
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
rs121913616
MPL
0.790 0.120 1 43349337 missense variant TG/AA mnv 8
rs12342421
JAK2 ; INSL6
0.851 0.080 9 5065750 intron variant G/C snv 0.23 5
rs10815148
JAK2 ; INSL6
0.882 0.080 9 5057284 intron variant T/A snv 0.33 3
rs10974947
INSL6 ; JAK2
0.882 0.080 9 5072846 intron variant G/A snv 0.23 3
rs121912473
JAK2 ; INSL6
0.925 0.080 9 5070026 missense variant AA/TT mnv 3
rs12339666
INSL6 ; JAK2
0.925 0.080 9 5063296 intron variant G/T snv 0.34 3
rs2201862 0.925 0.080 3 168930251 downstream gene variant T/C snv 0.63 3
rs318699
RGL3
0.882 0.080 19 11390564 intron variant A/G snv 0.73 3
rs4495487
INSL6 ; JAK2
0.925 0.080 9 5072798 intron variant T/C snv 0.23 3
rs1200469268
ABCA1
0.925 0.080 9 104830968 missense variant C/A snv 7.0E-06 2
rs3808850
JAK2
0.925 0.080 9 4983311 upstream gene variant T/A;C snv 2
rs7046736
JAK2 ; INSL6
0.925 0.080 9 5015732 intron variant C/A snv 0.39 2
rs11999802 1.000 0.080 9 5189773 upstream gene variant T/G snv 0.33 1
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs766642690
MPL
1.000 0.080 1 43352635 missense variant T/C;G snv 4.0E-06 1
rs772889171
RUNX1
0.925 0.080 21 34834487 missense variant G/A snv 4.0E-06 2