Disease: Malignant neoplasm of lung
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1235162
GABBR1
0.827 0.280 6 29569447 intron variant A/G snv 6.0E-02 6
rs1270942
CFB ; CYP21A2
0.742 0.440 6 31951083 non coding transcript exon variant A/G snv 7.5E-02 6
rs1794282 0.807 0.320 6 32698749 intergenic variant C/T snv 6.4E-02 6
rs2187668
LOC107986589 ; HLA-DQA2 ; HLA-DQA1
0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 10
rs2233956
PSORS1C1 ; C6orf15
0.827 0.320 6 31113428 upstream gene variant T/C snv 0.12 3
rs2395185
HLA-DRB9
0.724 0.360 6 32465390 intron variant G/T snv 0.29 8
rs2517598
TRIM31 ; TRIM31-AS1
0.851 0.280 6 30112497 synonymous variant G/A snv 0.14 0.13 4
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 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
rs2844773
HCG17 ; TRIM26BP
0.882 0.240 6 30239718 intron variant C/A snv 0.11 3
rs3094054 0.807 0.280 6 30365728 upstream gene variant G/A;T snv 5
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 2
rs3094694 0.925 0.200 6 30484127 upstream gene variant T/C snv 0.16 2
rs3099844
MICB-DT
0.732 0.400 6 31481199 non coding transcript exon variant C/A snv 0.11 9
rs3117582
BAG6 ; APOM
0.716 0.440 6 31652743 intron variant T/G snv 7.1E-02 6
rs3129763 0.827 0.280 6 32623148 TF binding site variant G/A snv 0.23 6
rs3129791
HCG15
0.827 0.280 6 28986516 intron variant G/A snv 5.3E-02 4
rs3130350 0.827 0.280 6 30360062 upstream gene variant G/T snv 7.1E-02 5
rs3130380
HCG18 ; HCG17
0.807 0.280 6 30311353 intron variant G/A snv 6.6E-02 10
rs3130544 0.807 0.360 6 31090563 intergenic variant C/A snv 7.4E-02 6
rs3130564
PSORS1C1
0.790 0.360 6 31133897 intron variant C/T snv 0.14 5
rs3131379
MSH5 ; MSH5-SAPCD1
0.752 0.440 6 31753256 intron variant G/A snv 6.4E-02 7.9E-02 6