Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1056836
CYP1B1
0.581 0.680 2 38071060 missense variant G/C snv 0.51 58
rs1057519045
FGFR2
0.851 0.160 10 121498522 missense variant T/G snv 6
rs1057519720
BRAF
0.851 0.080 7 140781602 missense variant CC/AA;GA mnv 4
rs1057519728
MAP2K1
0.851 0.120 15 66435103 missense variant T/A;C;G snv 5
rs1057519731
MAP2K1
0.925 0.040 15 66436816 missense variant G/C snv 2
rs1057519747
TP53
0.716 0.280 17 7675094 missense variant A/C;G;T snv 23
rs1057519781
ALK
0.807 0.160 2 29209816 missense variant C/G snv 9
rs1057519782
ALK
1.000 0.040 2 29220734 missense variant G/T snv 1
rs1057519783
ALK
0.851 0.080 2 29220747 missense variant C/T snv 10
rs1057519784
ALK
0.827 0.080 2 29220765 missense variant G/T snv 7
rs1057519785
ALK
1.000 0.040 2 29222404 missense variant A/C snv 2
rs1057519786
ARAF
0.882 0.160 X 47566722 missense variant C/G;T snv 5
rs1057519787
ERBB2
1.000 0.040 17 39711952 missense variant G/A;C snv 2
rs1057519788
ROS1
0.925 0.080 6 117317184 missense variant C/T snv 6
rs1057519816
ERBB2
0.763 0.200 17 39711955 missense variant C/A;T snv 14
rs1057519847
EGFR
0.570 0.560 7 55191821 missense variant CT/AG mnv 72
rs1057519848
EGFR
0.570 0.560 7 55191822 missense variant TG/GT mnv 72
rs1057519854
FGFR2
0.882 0.080 10 121488063 missense variant A/T snv 7
rs1057519856
MAP2K1
0.925 0.040 15 66436815 missense variant T/A snv 2
rs1057519861
EGFR ; EGFR-AS1
0.776 0.080 7 55181398 missense variant T/A snv 15
rs1057519876
ARAF
0.882 0.160 X 47566721 missense variant T/G snv 3
rs1057519877
B2M ; PATL2
0.763 0.280 15 44711549 start lost G/A snv 10
rs1057519879
PATL2 ; B2M
0.763 0.280 15 44711548 start lost T/C;G snv 10
rs1057519881
CDKN2A
0.776 0.240 9 21971111 missense variant T/C snv 8
rs1057519883
CDKN2A
0.742 0.280 9 21971120 missense variant C/G;T snv 14