Disease: Malignant neoplasm of lung
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3094694 0.925 0.200 6 30484127 upstream gene variant T/C snv 0.16 2
rs2844773
HCG17 ; TRIM26BP
0.882 0.240 6 30239718 intron variant C/A snv 0.11 3
rs3094073
HLA-L ; HCG17
0.882 0.240 6 30263447 non coding transcript exon variant G/A snv 0.12 0.12 3
rs3094127
FLOT1
0.925 0.200 6 30729670 intron variant A/G snv 0.27 3
rs1052486
BAG6
0.851 0.200 6 31642909 missense variant A/G snv 0.51 0.44 4
rs2517598
TRIM31 ; TRIM31-AS1
0.851 0.280 6 30112497 synonymous variant G/A snv 0.14 0.13 4
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
rs9262143
PPP1R18
0.851 0.240 6 30685004 missense variant C/G;T snv 4.1E-06; 6.1E-02 4
rs2233956
PSORS1C1 ; C6orf15
0.827 0.320 6 31113428 upstream gene variant T/C snv 0.12 5
rs2523987
TRIM31-AS1 ; TRIM31
0.827 0.280 6 30112216 intron variant A/C snv 9.2E-02 5
rs2523989
TRIM31 ; TRIM31-AS1
0.827 0.280 6 30110498 missense variant C/T snv 0.12 0.12 5
rs3129791
HCG15
0.827 0.280 6 28986516 intron variant G/A snv 5.3E-02 5
rs3130350 0.827 0.280 6 30360062 upstream gene variant G/T snv 7.1E-02 5
rs1235162
GABBR1
0.827 0.280 6 29569447 intron variant A/G snv 6.0E-02 6
rs1794282 0.807 0.320 6 32698749 intergenic variant C/T snv 6.4E-02 6
rs3094054 0.807 0.280 6 30365728 upstream gene variant G/A;T snv 6
rs3129763 0.827 0.280 6 32623148 TF binding site variant G/A snv 0.23 6
rs3132610
ABCF1
0.807 0.280 6 30576624 intron variant A/G snv 7.4E-02 6
rs3132685
HLA-A ; HCG9
0.807 0.320 6 29978172 intron variant G/A;T snv 6
rs558702
C2 ; ZBTB12 ; CYP21A2
0.807 0.320 6 31902549 intron variant G/A snv 7.7E-02 6
rs7750641
TCF19
0.807 0.360 6 31161533 missense variant C/T snv 7.0E-02 7.6E-02 6
rs7762279 0.807 0.360 6 32787513 intergenic variant T/C snv 8.4E-02 6
rs3130564
PSORS1C1
0.790 0.360 6 31133897 intron variant C/T snv 0.14 7
rs3132580
HCG21 ; SFTA2 ; MUCL3
0.790 0.360 6 30952347 missense variant G/A snv 8.0E-02 9.3E-02 7