Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913459
ABL1
0.672 0.160 9 130872896 missense variant C/T snv 25
rs121913615
MPL
0.683 0.240 1 43349338 missense variant G/C;T snv 8.0E-06 25
rs1275561861
HLA-A
0.672 0.360 6 29944350 missense variant G/A snv 23
rs1448674651
TYMS ; ENOSF1
0.667 0.560 18 671384 missense variant G/A;C snv 4.0E-06 23
rs3731249
CDKN2A
0.683 0.320 9 21970917 missense variant C/A;G;T snv 2.1E-02 23
rs61754966
NBN
0.701 0.280 8 89978293 missense variant T/C;G snv 1.2E-03 23
rs1039659576
MTR
0.689 0.520 1 236803473 missense variant A/G snv 21
rs17855750
IL27
0.695 0.480 16 28503907 missense variant A/C;T snv 6.4E-02; 4.0E-06 21
rs2295080
MTOR
0.695 0.320 1 11262571 upstream gene variant G/C;T snv 20
rs34767364
NBN
0.701 0.280 8 89971232 missense variant G/A;C snv 2.5E-03 20
rs1206846668
FOLH1
0.724 0.400 11 49185773 missense variant G/A snv 4.1E-06 16
rs3822214
KIT
0.732 0.240 4 54727298 missense variant A/C;G;T snv 7.7E-02; 8.0E-06 13
rs755001634
FOLH1
0.763 0.280 11 49154384 stop gained G/A snv 1.2E-05 13
rs35201683
HFE
0.732 0.360 6 26094205 stop gained C/A;T snv 1.4E-03 12
rs780246573
HFE ; LOC108783645
0.732 0.360 6 26092860 stop gained C/G;T snv 4.0E-06; 8.0E-06 12
rs200928781
CHEK2
0.752 0.240 22 28695800 missense variant T/A;C;G snv 2.4E-05 11
rs213210
MIR219A1 ; RING1
0.742 0.240 6 33208047 upstream gene variant A/C;G snv 11
rs3824662
GATA3
0.752 0.320 10 8062245 intron variant C/A;T snv 11
rs3731217
CDKN2A
0.763 0.320 9 21984662 intron variant A/C;T snv 10
rs1057519753
JAK1
0.763 0.120 1 64846664 missense variant C/A snv 9
rs10828317
PIP4K2A
0.776 0.280 10 22550699 missense variant T/C snv 9
rs1142345
TPMT
0.776 0.280 6 18130687 missense variant T/C;G snv 3.7E-02 9
rs2069727
IFNG ; IFNG-AS1
0.763 0.320 12 68154443 intron variant T/A;C snv 9
rs111033563
LOC108783645 ; HFE
0.776 0.240 6 26092916 missense variant A/C snv 4.0E-06 8
rs121913488
FLT3
0.807 0.120 13 28018505 missense variant C/A;G;T snv 7