Disease: Carcinoma of lung
Source: BEFREE ×
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
rs10054203
TERT
0.882 0.080 5 1279849 intron variant G/A;C;T snv 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 4
rs10213865
LOC105374724 ; IL7R
0.827 0.120 5 35857748 intron variant A/C;T snv 5
rs10254120
PMS2
0.851 0.080 7 6005996 missense variant C/A;G;T snv 7.2E-02 5
rs1035938
BICRA
0.776 0.120 19 47680514 missense variant C/G;T snv 0.29 8
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1042711
ADRB2
0.827 0.120 5 148826785 5 prime UTR variant C/A;G;T snv 4.2E-06; 0.68 5
rs1043973338
IL1B
0.882 0.080 2 112830483 missense variant A/C snv 3
rs1043994
NOTCH3
0.827 0.120 19 15192033 synonymous variant T/A;C snv 4.0E-06; 0.85 7
rs1044396
CHRNA4
0.742 0.240 20 63349782 missense variant G/A;C snv 0.47; 6.1E-05 17
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1046175
PAOX
0.851 0.080 10 133391446 stop gained C/A;G;T snv 1.2E-05; 0.88 4
rs104886003
PIK3CA
0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 43
rs104886026
EGFR
0.851 0.080 7 55200333 missense variant G/A snv 4
rs10508266 0.882 0.080 10 3797822 intergenic variant G/A;T snv 3
rs1053566
MAP2K7
0.882 0.080 19 7911079 missense variant C/T snv 3
rs1057519697
ALK
0.776 0.120 2 29220830 missense variant A/C snv 10
rs1057519729
MAP2K1
0.827 0.080 15 66435113 missense variant A/C snv 5
rs1057519784
ALK
0.827 0.080 2 29220765 missense variant G/T snv 6
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 3
rs1057519861
EGFR ; EGFR-AS1
0.776 0.080 7 55181398 missense variant T/A snv 15