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
rs1050171
EGFR ; EGFR-AS1
0.851 0.120 7 55181370 missense variant G/A;C snv 0.52; 4.0E-06 6
rs909797662
EGFR
0.790 0.120 7 55191837 missense variant G/A snv 8
rs7086803
VTI1A
0.763 0.160 10 112738717 intron variant G/A snv 0.20 9
rs369410616
MUTYH
0.752 0.280 1 45329400 missense variant C/T snv 2.0E-05 2.8E-05 10
rs941759532
ERCC4
0.763 0.240 16 13932175 missense variant C/G snv 11
rs10012
CYP1B1 ; CYP1B1-AS1
0.716 0.280 2 38075247 missense variant G/C snv 0.31 0.36 16
rs121913238
KRAS
0.732 0.240 12 25227343 missense variant G/C;T snv 17
rs10165970
NPAS2
0.708 0.320 2 100840527 intron variant G/A snv 0.16 18
rs10519097
RORA
0.708 0.320 15 60997989 intron variant C/T snv 0.13 18
rs11943456
TMEM165
0.708 0.320 4 55410167 intron variant T/C snv 0.42 18
rs17024869
NPAS2
0.708 0.320 2 100843581 intron variant T/C snv 8.3E-02 18
rs28360071
XRCC4
0.708 0.240 5 83142293 intron variant GATGAGGAAACTAACTCTCAGTGGTGTTTA/- delins 0.48 18
rs7581886
NPAS2
0.708 0.320 2 100964784 intron variant C/T snv 0.92 18
rs16917496
KMT5A
0.689 0.360 12 123409283 3 prime UTR variant C/G;T snv 21
rs2296147
BIVM-ERCC5 ; ERCC5
0.695 0.280 13 102846025 5 prime UTR variant T/C snv 0.38 21
rs187115
CD44
0.695 0.320 11 35154612 intron variant T/C snv 0.37 22
rs189037
ATM ; NPAT
0.689 0.400 11 108223106 5 prime UTR variant G/A snv 0.49 22
rs895520
NPAS2
0.689 0.320 2 100961475 intron variant G/A snv 0.35 23
rs121913338
BRAF
0.677 0.400 7 140753354 missense variant T/A;C;G snv 24
rs3219489
MUTYH
0.672 0.360 1 45331833 missense variant C/A;G snv 0.29 0.27 24
rs2298881
ERCC1
0.653 0.400 19 45423658 intron variant C/A;T snv 25
rs2839698
MRPL23 ; MIR675 ; H19
0.662 0.520 11 1997623 non coding transcript exon variant G/A snv 0.41 25
rs876658657
MLH1
0.677 0.280 3 37020356 missense variant A/G snv 4.0E-06 25
rs1143623
IL1B
0.677 0.440 2 112838252 upstream gene variant C/G snv 0.24 29
rs1800440
CYP1B1
0.653 0.440 2 38070996 missense variant T/C;G snv 0.15; 4.0E-06 29