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
rs1002481
REV3L ; MFSD4B
0.882 0.080 6 111390819 intron variant T/A;G snv 3
rs10040363
XRCC4
0.882 0.080 5 83177826 intron variant A/G snv 0.50 3
rs10053847
IL7R
0.882 0.080 5 35878038 3 prime UTR variant G/A snv 0.13 3
rs10054203
TERT
0.882 0.080 5 1279849 intron variant G/A;C;T snv 3
rs1014264982
HMG20B
0.882 0.080 19 3577038 missense variant G/A;C snv 6.8E-06 7.0E-06 3
rs10187911
NRXN1
0.882 0.080 2 50420809 intron variant C/A;G;T snv 3
rs1019340046
TP53
0.882 0.080 17 7674225 missense variant C/T snv 5
rs10244817
POT1
0.882 0.080 7 124827416 intron variant T/C snv 0.22 3
rs10254120
PMS2
0.851 0.080 7 6005996 missense variant C/A;G;T snv 7.2E-02 5
rs1026411
LOC105375751 ; PCAT1
0.827 0.080 8 127014165 intron variant G/A;C snv 0.25 5
rs10412613
PPP2R1A
0.882 0.080 19 52209575 intron variant G/A snv 0.63 3
rs1043973338
IL1B
0.882 0.080 2 112830483 missense variant A/C snv 3
rs1046175
PAOX
0.851 0.080 10 133391446 stop gained C/A;G;T snv 1.2E-05; 0.88 4
rs10487372
CFTR ; CFTR-AS1
0.882 0.080 7 117560845 intron variant C/T snv 0.13 3
rs104886026
EGFR
0.851 0.080 7 55200333 missense variant G/A snv 4
rs1049337
CAV1
0.882 0.080 7 116560533 3 prime UTR variant C/T snv 0.25 3
rs10508266 0.882 0.080 10 3797822 intergenic variant G/A;T snv 3
rs10512948 0.882 0.080 5 8233238 intron variant T/C snv 0.15 3
rs10519203
HYKK
0.851 0.080 15 78521704 intron variant G/A snv 0.67 8
rs10519717
LOC105377462
0.851 0.080 4 144559188 intron variant T/C snv 0.21 4
rs1053566
MAP2K7
0.882 0.080 19 7911079 missense variant C/T snv 3
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
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