Disease: Adenocarcinoma of lung (disorder)
Source: CLINVAR ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519786
ARAF
0.882 0.160 X 47566722 missense variant C/G;T snv 3
rs1057519876
ARAF
0.882 0.160 X 47566721 missense variant T/G snv 3
rs1057519908
MAP2K1
0.882 0.120 15 66435105 missense variant T/G snv 4
rs104894340
CDK4
0.827 0.200 12 57751647 missense variant C/A;T snv 5
rs1057519728
MAP2K1
0.851 0.120 15 66435103 missense variant T/A;C;G snv 5
rs1057519918
CASC11 ; MYC
0.851 0.200 8 127738390 missense variant C/T snv 5
rs750664148
CASC11 ; MYC
0.851 0.200 8 127738434 missense variant A/C;G snv 5
rs1057519909
MAP2K1
0.790 0.240 15 66435116 missense variant A/C snv 6
rs11547328
CDK4
0.701 0.360 12 57751648 missense variant G/A;T snv 4.0E-06 6
rs121913366
BRAF
0.763 0.400 7 140753345 missense variant A/C;T snv 6
rs756091827
MYC ; CASC11
0.851 0.200 8 127738435 missense variant C/G;T snv 6
rs1057519881
CDKN2A
0.776 0.240 9 21971111 missense variant T/C snv 8
rs121913365
BRAF
0.776 0.320 7 140753332 missense variant T/A;G snv 8
rs121913385
CDKN2A
0.763 0.240 9 21971112 missense variant G/A;C snv 8
rs121913469
ERBB2
0.763 0.240 17 39723966 missense variant TT/CC mnv 8
rs121913351
BRAF
0.776 0.240 7 140781611 missense variant C/A;G;T snv 4.0E-06 9
rs121913370
BRAF
0.763 0.360 7 140753393 missense variant T/C;G snv 9
rs121913409
CTNNB1
0.708 0.400 3 41224646 missense variant C/A;G;T snv 9
rs121913413
CTNNB1
0.763 0.240 3 41224634 missense variant C/A;T snv 9
rs180177040
BRAF
0.790 0.360 7 140754187 missense variant T/C;G snv 9
rs34968276
CDKN2A
0.776 0.240 9 21971110 stop gained G/A;C;T snv 9
rs869025608
MAP2K1
0.763 0.400 15 66435117 missense variant G/C;T snv 9
rs1023835002
B2M ; PATL2
0.763 0.280 15 44711547 start lost A/G;T snv 10
rs1057519877
B2M ; PATL2
0.763 0.280 15 44711549 start lost G/A snv 10
rs1057519879
PATL2 ; B2M
0.763 0.280 15 44711548 start lost T/C;G snv 10