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
rs1012477
PER3
0.827 0.160 1 7798075 intron variant G/C snv 0.16 8
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
rs11568820
VDR
0.672 0.480 12 47908762 intron variant C/T snv 0.38 27
rs11632964
SMAD3
1.000 0.080 15 67071235 intron variant C/G;T snv 2
rs11943456
TMEM165
0.708 0.320 4 55410167 intron variant T/C snv 0.42 18
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs17024869
NPAS2
0.708 0.320 2 100843581 intron variant T/C snv 8.3E-02 18
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs187115
CD44
0.695 0.320 11 35154612 intron variant T/C snv 0.37 22
rs2131877
XXYLT1
0.827 0.080 3 195137645 intron variant G/A snv 0.20 6
rs2245214
ATG5
0.827 0.240 6 106214866 intron variant C/G snv 0.42 6
rs2267437
DESI1 ; XRCC6
0.724 0.320 22 41620695 intron variant C/A;G snv 19
rs2279744
MDM2
0.605 0.640 12 68808800 intron variant T/G snv 0.31 48
rs3021094
IL10 ; IL19
0.827 0.360 1 206771607 intron variant T/G snv 8.0E-02 8
rs3743073
CHRNA3
0.807 0.120 15 78617197 intron variant G/T snv 0.61 11
rs3761548
FOXP3
0.620 0.680 X 49261784 intron variant G/A;T snv 42
rs401681
CLPTM1L
0.620 0.640 5 1321972 intron variant C/T snv 0.48 42
rs4402960
IGF2BP2
0.724 0.400 3 185793899 intron variant G/T snv 0.38 21
rs4645981
CASP9 ; DNAJC16
0.790 0.160 1 15524988 intron variant G/A;C snv 11
rs471692
TOP2A
0.925 0.080 17 40400518 intron variant T/A;C snv 0.79 3
rs7164773
RORA
0.790 0.240 15 60775749 intron variant C/A;T snv 10
rs7372209
CTDSPL ; MIR26A1
0.807 0.160 3 37969217 intron variant T/C snv 0.77 7
rs744166
STAT3
0.689 0.560 17 42362183 intron variant A/G snv 0.48 22
rs7581886
NPAS2
0.708 0.320 2 100964784 intron variant C/T snv 0.92 18