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
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs863225283
ALK
0.925 0.080 2 29213993 missense variant A/C snv 4
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs1057519975
TP53
0.649 0.480 17 7675209 missense variant A/C;G;T snv 34
rs10735810
VDR
0.662 0.640 12 47879112 start lost A/C;G;T snv 26
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs281864719
ALK
0.763 0.240 2 29220831 missense variant A/C;G;T snv 14
rs2032582
ABCB1
0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs1137101
LEPR
0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs11615
ERCC1
0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs121913246
MET
0.827 0.200 7 116783360 missense variant A/G snv 7
rs1430452530
HIF1A-AS3 ; HIF1A
0.851 0.160 14 61721518 missense variant A/G snv 4.0E-06 5
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs201661522
ABCB1
1.000 0.080 7 87539293 missense variant A/G snv 6.4E-05 1.0E-04 2
rs2227928
ATR
0.851 0.200 3 142562770 missense variant A/G snv 0.55 0.63 6
rs2853669
TERT
0.649 0.320 5 1295234 upstream gene variant A/G snv 0.25 35
rs3746444
MIR499A ; MIR499B ; MYH7B ; LOC107985393
0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs4809957
CYP24A1
0.763 0.240 20 54154632 3 prime UTR variant A/G snv 0.29 10
rs4880
SOD2
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs5498
ICAM4 ; ICAM1
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs731236
VDR
0.542 0.760 12 47844974 synonymous variant A/G snv 0.33 0.34 81
rs744166
STAT3
0.689 0.560 17 42362183 intron variant A/G snv 0.48 22