Disease: Malignant neoplasm of lung
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1794282 0.807 0.320 6 32698749 intergenic variant C/T snv 6.4E-02 6
rs2746150 0.851 0.240 6 29474924 downstream gene variant C/T snv 5.3E-02 4
rs2844659 0.851 0.280 6 30856755 intergenic variant C/G;T snv 4
rs3094054 0.807 0.280 6 30365728 upstream gene variant G/A;T snv 6
rs3094694 0.925 0.200 6 30484127 upstream gene variant T/C snv 0.16 2
rs3129763 0.827 0.280 6 32623148 TF binding site variant G/A snv 0.23 6
rs3130350 0.827 0.280 6 30360062 upstream gene variant G/T snv 7.1E-02 5
rs3130544 0.807 0.360 6 31090563 intergenic variant C/A snv 7.4E-02 10
rs7762279 0.807 0.360 6 32787513 intergenic variant T/C snv 8.4E-02 6
rs3132610
ABCF1
0.807 0.280 6 30576624 intron variant A/G snv 7.4E-02 6
rs2070600
AGER
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs1052486
BAG6
0.851 0.200 6 31642909 missense variant A/G snv 0.51 0.44 4
rs3117582
BAG6 ; APOM
0.716 0.440 6 31652743 intron variant T/G snv 7.1E-02 14
rs558702
C2 ; ZBTB12 ; CYP21A2
0.807 0.320 6 31902549 intron variant G/A snv 7.7E-02 6
rs1270942
CFB ; CYP21A2
0.742 0.440 6 31951083 non coding transcript exon variant A/G snv 7.5E-02 11
rs4673
CYBA
0.653 0.600 16 88646828 missense variant A/G;T snv 0.70 32
rs763110
FASLG
0.653 0.560 1 172658358 upstream gene variant C/T snv 0.49 30
rs3094127
FLOT1
0.925 0.200 6 30729670 intron variant A/G snv 0.27 3
rs1235162
GABBR1
0.827 0.280 6 29569447 intron variant A/G snv 6.0E-02 6
rs3129791
HCG15
0.827 0.280 6 28986516 intron variant G/A snv 5.3E-02 5
rs2844773
HCG17 ; TRIM26BP
0.882 0.240 6 30239718 intron variant C/A snv 0.11 3
rs3130380
HCG18 ; HCG17
0.807 0.280 6 30311353 intron variant G/A snv 6.6E-02 10
rs3132580
HCG21 ; SFTA2 ; MUCL3
0.790 0.360 6 30952347 missense variant G/A snv 8.0E-02 9.3E-02 7
rs3132685
HLA-A ; HCG9
0.807 0.320 6 29978172 intron variant G/A;T snv 6
rs2395185
HLA-DRB9
0.724 0.360 6 32465390 intron variant G/T snv 0.29 17