Disease: Primary malignant neoplasm of lung
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10213865
LOC105374724 ; IL7R
0.827 0.120 5 35857748 intron variant A/C;T snv 5
rs1026411
LOC105375751 ; PCAT1
0.827 0.080 8 127014165 intron variant G/A;C snv 0.25 5
rs104886026
EGFR
0.851 0.080 7 55200333 missense variant G/A snv 4
rs1051753269
EGFR
0.790 0.120 7 55174029 missense variant G/A snv 7.0E-06 7
rs1056836
CYP1B1
0.581 0.680 2 38071060 missense variant G/C snv 0.51 58
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
rs1057519861
EGFR ; EGFR-AS1
0.776 0.080 7 55181398 missense variant T/A snv 15
rs1057519975
TP53
0.649 0.480 17 7675209 missense variant A/C;G;T snv 34
rs1062980
IREB2
0.827 0.080 15 78500185 3 prime UTR variant T/C snv 0.39 8
rs1064607
LPP
0.827 0.200 3 188877884 3 prime UTR variant G/C snv 0.46 5
rs10877887
LINC01465 ; MIRLET7I
0.701 0.440 12 62603400 non coding transcript exon variant T/C snv 0.42 18
rs10937405
TP63
0.807 0.080 3 189665394 intron variant C/T snv 0.38 9
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs11568820
VDR
0.672 0.480 12 47908762 intron variant C/T snv 0.38 27
rs121434568
EGFR
0.568 0.560 7 55191822 missense variant T/A;G snv 73
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs121913465
EGFR ; EGFR-AS1
0.763 0.160 7 55181312 missense variant G/T snv 11
rs121913469
ERBB2
0.763 0.240 17 39723966 missense variant TT/CC mnv 11
rs121913530
KRAS
0.583 0.640 12 25245351 missense variant C/A;G;T snv 63
rs1258159645
NQO1
0.630 0.600 16 69711128 missense variant G/A snv 7.0E-06 37
rs1275824108
CDKN3
0.851 0.080 14 54399922 missense variant A/G snv 7.0E-06 5
rs12910984
CHRNA3
0.827 0.080 15 78599285 intron variant G/A;C;T snv 8
rs12914385
CHRNA3
0.790 0.160 15 78606381 intron variant C/A;T snv 18