Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4858647 0.925 0.080 3 24749884 intron variant C/A;G;T snv 2
rs1057519752
MPL
1.000 0.080 1 43349307 missense variant A/C;G;T snv 1
rs12340895
INSL6 ; JAK2
1.000 0.080 9 5076691 intron variant C/A;G snv 1
rs59384377
INSL6 ; JAK2
1.000 0.080 9 5005034 intron variant A/T snv 0.26 1
rs16754
WT1
0.732 0.240 11 32396399 synonymous variant T/C snv 0.24; 4.0E-06 0.17 15
rs1441084781
TLR4
1.000 0.080 9 117712543 missense variant G/A;T snv 4.0E-06 1
rs121913529
KRAS
0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144
rs556915505
MECOM
0.851 0.080 3 169143780 missense variant T/C snv 4.0E-06 7.0E-06 5
rs17849241
SOCS3 ; LOC101928674
0.925 0.080 17 78358688 missense variant G/C;T snv 4.1E-06; 2.1E-04 3
rs3733609
TET2 ; TET2-AS1
1.000 0.080 4 105269705 missense variant T/A;C snv 6.4E-06; 3.4E-02 2
rs121913237
NRAS
0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 50
rs562533120
HBS1L
0.882 0.080 6 134966397 missense variant A/C snv 8.0E-06 3
rs121913615
MPL
0.683 0.240 1 43349338 missense variant G/C;T snv 8.0E-06 25
rs529311209
SGSM3
0.925 0.120 22 40409754 missense variant G/A;C;T snv 3.3E-05; 8.2E-06 2
rs562015640
PTEN
0.742 0.360 10 87960957 stop gained A/G;T snv 1.2E-05 16
rs764634461
JAK2 ; INSL6
1.000 0.080 9 5072516 missense variant T/G snv 1.2E-05 2.8E-05 1
rs778767225
MOK
0.851 0.200 14 102231805 missense variant C/A snv 2.4E-05 7.0E-06 4
rs121913502
IDH2
0.708 0.320 15 90088702 missense variant C/A;T snv 3.2E-05 19
rs201478192
KIDINS220
0.790 0.200 2 8731667 missense variant C/A snv 2.4E-04 2.6E-04 12
rs77375493
INSL6 ; JAK2
0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 187
rs17292650
MPL
0.882 0.120 1 43338136 missense variant G/T snv 3.5E-03 1.4E-02 3
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262