Disease: Non-Small Cell Lung Carcinoma
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1048977
CDA
1.000 0.080 1 20618562 synonymous variant C/T snv 0.31 0.34 2
rs1057519783
ALK
0.851 0.080 2 29220747 missense variant C/T snv 10
rs1057519784
ALK
0.827 0.080 2 29220765 missense variant G/T snv 7
rs1057519788
ROS1
0.925 0.080 6 117317184 missense variant C/T snv 6
rs1057519861
EGFR ; EGFR-AS1
0.776 0.080 7 55181398 missense variant T/A snv 15
rs11632964
SMAD3
1.000 0.080 15 67071235 intron variant C/G;T snv 2
rs1423493595
UBE2V1 ; TMEM189-UBE2V1
0.851 0.080 20 50082836 missense variant G/A snv 4.0E-06 7.0E-06 5
rs1564483
BCL2
1.000 0.080 18 63127421 3 prime UTR variant C/T snv 0.22 4
rs201661522
ABCB1
1.000 0.080 7 87539293 missense variant A/G snv 6.4E-05 1.0E-04 2
rs2131877
XXYLT1
0.827 0.080 3 195137645 intron variant G/A snv 0.20 6
rs41281081
MET
1.000 0.080 7 116796211 3 prime UTR variant G/A snv 2.5E-03 3
rs471692
TOP2A
0.925 0.080 17 40400518 intron variant T/A;C snv 0.79 3
rs55985569
MET
0.925 0.080 7 116699588 missense variant G/A;T snv 3.7E-03 3
rs7040869 1.000 0.080 9 99072866 downstream gene variant G/A snv 0.11 2
rs751306825
ALK
0.925 0.080 2 29220759 missense variant G/A;T snv 4.0E-06 4
rs759435862
KIDINS220
0.925 0.080 2 8776852 missense variant C/A;T snv 2.0E-05 5
rs760943842
ZNF436
0.851 0.080 1 23362976 missense variant G/A snv 4.0E-05 1.4E-05 5
rs76322625
MET
1.000 0.080 7 116798111 3 prime UTR variant C/A;T snv 3
rs767935771
AXL
0.827 0.080 19 41259690 missense variant T/C snv 1.6E-05 5.6E-05 6
rs779179533
TP63
1.000 0.080 3 189808322 missense variant G/C snv 4.0E-06 2
rs863225283
ALK
0.925 0.080 2 29213993 missense variant A/C snv 4
rs10079250
CSF1R
0.827 0.120 5 150070569 missense variant T/C snv 9.9E-02 8.6E-02 7
rs1057519698
ALK
0.827 0.120 2 29222347 missense variant A/G;T snv 8
rs121913428
EGFR
0.827 0.120 7 55174015 missense variant G/A;C snv 6
rs2279574
DUSP6
0.827 0.120 12 89351700 missense variant C/A;T snv 0.52 8