Disease: Malignant neoplasm of lung
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1052486
BAG6
0.851 0.200 6 31642909 missense variant A/G snv 0.51 0.44 4
rs1053566
MAP2K7
0.882 0.080 19 7911079 missense variant C/T snv 3
rs1056827
CYP1B1 ; CYP1B1-AS1
0.683 0.400 2 38075034 missense variant C/A snv 0.32 0.35 24
rs1056836
CYP1B1
0.581 0.680 2 38071060 missense variant G/C snv 0.51 58
rs1057519697
ALK
0.776 0.120 2 29220830 missense variant A/C snv 12
rs1057519729
MAP2K1
0.827 0.080 15 66435113 missense variant A/C snv 6
rs1057519784
ALK
0.827 0.080 2 29220765 missense variant G/T snv 7
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
rs1057519857
ERBB2 ; MIR4728
0.882 0.080 17 39724772 missense variant T/C snv 4
rs1057519861
EGFR ; EGFR-AS1
0.776 0.080 7 55181398 missense variant T/A snv 15
rs1057519911
MAPK1
0.776 0.160 22 21772875 missense variant C/T snv 10
rs1057519975
TP53
0.649 0.480 17 7675209 missense variant A/C;G;T snv 34
rs1057519984
TP53
0.882 0.080 17 7673777 missense variant G/C;T snv 3
rs1057520001
TP53
0.677 0.360 17 7674886 missense variant A/C;G snv 23
rs1057972
IL15
0.790 0.200 4 141733279 3 prime UTR variant A/T snv 0.54 7
rs1058808
ERBB2
0.658 0.360 17 39727784 missense variant C/G snv 0.61 0.52 27
rs1060501327
MUTYH
0.851 0.080 1 45332251 missense variant A/G snv 4
rs1060503291
APC
0.882 0.080 5 112835135 missense variant C/T snv 3
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs1062980
IREB2
0.827 0.080 15 78500185 3 prime UTR variant T/C snv 0.39 8
rs1063054
NBN ; OSGIN2
0.807 0.160 8 89934373 3 prime UTR variant T/G snv 0.32 6
rs1064607
LPP
0.827 0.200 3 188877884 3 prime UTR variant G/C snv 0.46 5
rs1065852
NDUFA6-DT ; LOC112268294 ; CYP2D6
0.695 0.360 22 42130692 missense variant G/A snv 0.21 0.19 19
rs10680577
RAB4B-EGLN2 ; EGLN2
0.776 0.160 19 40798690 intron variant -/TACT delins 10