Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121912473
JAK2 ; INSL6
0.925 0.080 9 5070026 missense variant AA/TT mnv 3
rs318699
RGL3
0.882 0.080 19 11390564 intron variant A/G snv 0.73 3
rs17849241
SOCS3 ; LOC101928674
0.925 0.080 17 78358688 missense variant G/C;T snv 4.1E-06; 2.1E-04 3
rs1200469268
ABCA1
0.925 0.080 9 104830968 missense variant C/A snv 7.0E-06 2
rs754190776
HBG2
0.925 0.080 11 5253350 missense variant G/A snv 8.0E-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
rs1253570532
RUNX1
0.925 0.080 21 34792289 missense variant G/A snv 7.0E-06 2
rs772889171
RUNX1
0.925 0.080 21 34834487 missense variant G/A snv 4.0E-06 2
rs11999802 1.000 0.080 9 5189773 upstream gene variant T/G snv 0.33 1
rs773475680
ABL1
1.000 0.080 9 130884139 missense variant C/T snv 4.0E-06 1
rs777342222
EGFR
1.000 0.080 7 55155925 missense variant T/C snv 4.0E-06 1
rs766642690
MPL
1.000 0.080 1 43352635 missense variant T/C;G snv 4.0E-06 1