Disease: Adenocarcinoma of lung (disorder)
Source: CLINVAR ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519854
FGFR2
0.882 0.080 10 121488063 missense variant A/T snv 5
rs1057519901
FGFR2
0.925 0.080 10 121498525 missense variant T/G snv 5
rs1057519963
SOS1
0.925 0.080 2 39054637 missense variant T/A snv 2
rs121913476
FGFR2
0.851 0.080 10 121498520 missense variant A/C;T snv 5
rs1057519045
FGFR2
0.851 0.160 10 121498522 missense variant T/G snv 6
rs1057519920
NFE2L2
0.790 0.160 2 177234232 missense variant C/A;G;T snv 7
rs1057519938
PIK3CA
0.776 0.160 3 179203764 missense variant A/C;T snv 10
rs1057519939
PIK3CA
0.776 0.160 3 179203763 missense variant A/C snv 10
rs1057519947
PPP2R1A
0.790 0.160 19 52212730 missense variant G/A snv 9
rs1057519999
TP53
0.763 0.160 17 7674247 missense variant T/C;G snv 12
rs121913284
PIK3CA
0.776 0.160 3 179203765 missense variant T/A;G snv 10
rs786201419
TP53
0.790 0.160 17 7675180 missense variant C/A;T snv 8
rs876660807
TP53
0.763 0.160 17 7674248 missense variant T/C snv 12
rs1057519926
PIK3CA
0.776 0.200 3 179210293 missense variant A/T snv 10
rs121913228
CTNNB1
0.742 0.200 3 41224621 missense variant T/C;G snv 11
rs121913399
CTNNB1
0.724 0.200 3 41224612 missense variant G/A;C snv 10
rs1057519886
CTNNB1
0.752 0.240 3 41224609 missense variant T/A;C;G snv 11
rs1057519895
FBXW7
0.724 0.240 4 152328232 missense variant C/A;G;T snv 14
rs1057519921
NFE2L2
0.763 0.240 2 177234231 missense variant T/C snv 7
rs1057519927
PIK3CA
0.716 0.240 3 179218295 missense variant A/C;G;T snv 18
rs1057519933
PIK3CA
0.790 0.240 3 179199156 missense variant A/G snv 11
rs1057519934
PIK3CA
0.790 0.240 3 179199158 missense variant G/C snv 11
rs1057519935
PIK3CA
0.790 0.240 3 179199157 missense variant A/G snv 11
rs1057519989
TP53
0.732 0.240 17 7674233 missense variant C/A;G;T snv 15
rs121913403
CTNNB1
0.683 0.240 3 41224622 missense variant C/A;G;T snv 13