Disease: Malignant neoplasm of lung
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 53
rs10849605
RAD52
0.882 0.080 12 955272 intron variant T/C snv 0.49 4
rs11568820
VDR
0.672 0.480 12 47908762 intron variant C/T snv 0.38 27
rs12587742
DCAF4
0.851 0.080 14 72926683 intron variant G/A snv 0.18 5
rs1412125
HMGB1
0.724 0.360 13 30467458 intron variant C/G;T snv 17
rs1447295
CASC8
0.658 0.400 8 127472793 intron variant A/C;T snv 29
rs1535045
CD40
0.742 0.360 20 46119460 intron variant C/A;G;T snv 12
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs16901979
PCAT1 ; CASC19
0.724 0.480 8 127112671 intron variant C/A snv 0.16 17
rs1799732
DRD2 ; LOC105369501
0.790 0.160 11 113475529 intron variant -/G delins 11
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs1800896
IL19 ; IL10
0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs2075786
TERT
0.790 0.360 5 1266195 intron variant A/G snv 0.55 8
rs2107425
MRPL23 ; H19
0.732 0.280 11 1999845 intron variant C/T snv 16
rs2131877
XXYLT1
0.827 0.080 3 195137645 intron variant G/A snv 0.20 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
rs3212948
ERCC1
0.776 0.160 19 45421104 intron variant G/C snv 0.53 10
rs3743073
CHRNA3
0.807 0.120 15 78617197 intron variant G/T snv 0.61 11
rs3787016
POLR2E
0.677 0.280 19 1090804 intron variant A/G snv 0.78 24
rs3817198
LSP1
0.790 0.280 11 1887776 intron variant T/C snv 0.26 8
rs401681
CLPTM1L
0.620 0.640 5 1321972 intron variant C/T snv 0.48 42
rs4645981
CASP9 ; DNAJC16
0.790 0.160 1 15524988 intron variant G/A;C snv 11
rs6721961
NFE2L2
0.672 0.520 2 177265309 intron variant T/C;G snv 0.89 24
rs762551
CYP1A2
0.701 0.400 15 74749576 intron variant C/A snv 0.67 23