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
rs10054203
TERT
0.882 0.080 5 1279849 intron variant G/A;C;T snv 3
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 53
rs10187911
NRXN1
0.882 0.080 2 50420809 intron variant C/A;G;T snv 3
rs10213865
LOC105374724 ; IL7R
0.827 0.120 5 35857748 intron variant A/C;T snv 5
rs10244817
POT1
0.882 0.080 7 124827416 intron variant T/C snv 0.22 3
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
rs10421768
HAMP
0.807 0.120 19 35281996 intron variant A/G snv 0.21 6
rs10487372
CFTR ; CFTR-AS1
0.882 0.080 7 117560845 intron variant C/T snv 0.13 3
rs10505477
CASC8 ; PCAT1 ; POU5F1B
0.658 0.400 8 127395198 intron variant A/G snv 0.40 31
rs10506868
VTI1A
0.716 0.160 10 112559621 intron variant C/T snv 3.1E-02 16
rs10511729
LOC101929563
0.742 0.240 9 23557229 intron variant T/G snv 0.35 11
rs10512948 0.882 0.080 5 8233238 intron variant T/C snv 0.15 3
rs10514231
ATG10
0.807 0.160 5 82011593 intron variant C/T snv 0.56 6
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
rs10680577
RAB4B-EGLN2 ; EGLN2
0.776 0.160 19 40798690 intron variant -/TACT delins 10
rs10937405
TP63
0.807 0.080 3 189665394 intron variant C/T snv 0.38 9
rs11072768
CHRNB4
0.882 0.080 15 78637136 intron variant T/C;G snv 4
rs11137037
ANGPT2 ; MCPH1
0.851 0.200 8 6538661 intron variant A/C snv 0.40 4
rs11196067
VTI1A
0.752 0.160 10 112709306 intron variant A/T snv 0.32 10
rs11196172
TCF7L2
0.708 0.200 10 112967084 intron variant G/A snv 0.13 18
rs11212592
ATM ; C11orf65
0.882 0.080 11 108348120 intron variant A/G snv 0.16 3