Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs17849241
SOCS3 ; LOC101928674
0.925 0.080 17 78358688 missense variant G/C;T snv 4.1E-06; 2.1E-04 3
rs1253570532
RUNX1
0.925 0.080 21 34792289 missense variant G/A snv 7.0E-06 2
rs780178275
VHL
0.851 0.200 3 10146586 missense variant C/T snv 8.0E-06 7
rs754190776
HBG2
0.925 0.080 11 5253350 missense variant G/A snv 8.0E-06 2
rs562533120
HBS1L
0.882 0.080 6 134966397 missense variant A/C snv 8.0E-06 3
rs1188383936
F2
0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 102
rs121913615
MPL
0.683 0.240 1 43349338 missense variant G/C;T snv 8.0E-06 25
rs775387828
NFE2
0.851 0.200 12 54293083 missense variant G/A snv 2.2E-05 7.0E-06 7
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
rs17576
MMP9
0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 73