Disease: Adenocarcinoma of lung (disorder)
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs867262025
PIK3CA
0.790 0.360 3 179221146 missense variant G/A snv 10
rs876658657
MLH1
0.677 0.280 3 37020356 missense variant A/G snv 4.0E-06 25
rs1057519895
FBXW7
0.724 0.240 4 152328232 missense variant C/A;G;T snv 17
rs121913482
FGFR3
0.630 0.680 4 1801837 missense variant C/T snv 45
rs7679673 0.677 0.440 4 105140377 intron variant C/A snv 0.50 28
rs867384286
FBXW7
0.732 0.240 4 152328233 missense variant G/A;C snv 4.3E-06 14
rs1862626 0.708 0.280 5 56737113 regulatory region variant G/T snv 0.68 17
rs401681
CLPTM1L
0.620 0.640 5 1321972 intron variant C/T snv 0.48 42
rs7725218
TERT
0.708 0.280 5 1282299 intron variant G/A snv 0.38 17
rs115392158
HLA-B
0.708 0.280 6 31347004 intron variant A/G snv 17
rs115707823 0.701 0.320 6 30374976 intergenic variant G/A snv 19
rs147527678 0.708 0.280 6 32699696 intergenic variant G/A;C snv 17
rs147680653 0.708 0.280 6 29785031 intergenic variant A/G snv 17
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
rs121434568
EGFR
0.568 0.560 7 55191822 missense variant T/A;G snv 73
rs121913351
BRAF
0.776 0.240 7 140781611 missense variant C/A;G;T snv 4.0E-06 9
rs121913355
BRAF
0.641 0.520 7 140781602 missense variant C/A;G;T snv 4.0E-06 42
rs121913357
BRAF
0.742 0.320 7 140781603 stop gained C/A;G;T snv 12
rs121913428
EGFR
0.827 0.120 7 55174015 missense variant G/A;C snv 6
rs121913444
EGFR
0.724 0.160 7 55191831 missense variant T/A;C;G snv 18
rs121913465
EGFR ; EGFR-AS1
0.763 0.160 7 55181312 missense variant G/T snv 11
rs150036236
EGFR
0.925 0.080 7 55191741 missense variant G/A snv 4.8E-05 3.5E-05 3
rs397517097
EGFR
0.851 0.080 7 55174777 missense variant T/C snv 4
rs1011970
CDKN2B-AS1
0.677 0.320 9 22062135 intron variant G/T snv 0.23 22