Disease: Malignant neoplasm of lung
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913316
STK11
1.000 0.080 19 1220489 missense variant A/T snv 2
rs10849605
RAD52
0.882 0.080 12 955272 intron variant T/C snv 0.49 4
rs139293
APOBEC3H
0.882 0.080 22 39100331 missense variant G/A;T snv 2.3E-04; 0.27 4
rs1467453450
FSD1L
0.882 0.080 9 105506513 missense variant A/G snv 7.0E-06 4
rs1862214 0.882 0.080 19 32544943 intergenic variant G/A;C snv 4
rs200487215
KARS1 ; TERF2IP
0.882 0.080 16 75647605 missense variant T/A;C snv 1.6E-05 4
rs774352237
TCHP
0.882 0.080 12 109908873 missense variant G/A snv 3.2E-05 2.1E-05 4
rs12587742
DCAF4
0.851 0.080 14 72926683 intron variant G/A snv 0.18 5
rs1275824108
CDKN3
0.851 0.080 14 54399922 missense variant A/G snv 7.0E-06 5
rs1329032366
PDLIM5
0.882 0.080 4 94654530 missense variant A/G snv 4.0E-06 5
rs1423493595
UBE2V1 ; TMEM189-UBE2V1
0.851 0.080 20 50082836 missense variant G/A snv 4.0E-06 7.0E-06 5
rs1430452530
HIF1A-AS3 ; HIF1A
0.851 0.160 14 61721518 missense variant A/G snv 4.0E-06 5
rs28382575
MMP11
0.851 0.120 22 23783502 synonymous variant T/C snv 2.2E-02 1.8E-02 5
rs2929973
CCN4
0.851 0.200 8 133230265 3 prime UTR variant G/T snv 0.85 5
rs374733251
MET
0.882 0.080 7 116740993 missense variant A/G snv 6.0E-05 7.7E-05 5
rs377444977
EGFR
0.882 0.080 7 55143443 missense variant G/A snv 5.2E-05 2.1E-05 5
rs533748068
ARHGEF2 ; MIR6738
0.851 0.080 1 155950962 missense variant C/A;T snv 4.3E-06 7.0E-06 5
rs760943842
ZNF436
0.851 0.080 1 23362976 missense variant G/A snv 4.0E-05 1.4E-05 5
rs775057330
CASC1
0.851 0.080 12 25149651 missense variant C/A;T snv 5
rs7969931
LRMP
0.851 0.080 12 25089661 missense variant C/A;G snv 1.6E-05; 0.75 5
rs121913387
CDKN2A
0.827 0.160 9 21971187 stop gained G/A;C snv 4.6E-06 6
rs1389500636
EGFR
0.827 0.080 7 55156796 missense variant G/A snv 6
rs1864182
ATG10
0.827 0.120 5 82253421 missense variant C/A;G snv 0.59 0.47 6
rs2071203
SEMA3B
0.827 0.120 3 50274469 missense variant C/T snv 0.12 9.9E-02 6
rs2131877
XXYLT1
0.827 0.080 3 195137645 intron variant G/A snv 0.20 6