Disease: Malignant neoplasm of lung
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs8321
ZNRD1
0.742 0.320 6 30064745 3 prime UTR variant A/C snv 5.4E-02 5.9E-02 11
rs2187668
LOC107986589 ; HLA-DQA2 ; HLA-DQA1
0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 10
rs3130380
HCG18 ; HCG17
0.807 0.280 6 30311353 intron variant G/A snv 6.6E-02 10
rs9261290
RNF39
0.807 0.280 6 30070870 3 prime UTR variant T/C;G snv 5.2E-02; 7.2E-06 10
rs3099844
MICB-DT
0.732 0.400 6 31481199 non coding transcript exon variant C/A snv 0.11 9
rs2395185
HLA-DRB9
0.724 0.360 6 32465390 intron variant G/T snv 0.29 8
rs389884
STK19 ; CYP21A2 ; DXO
0.776 0.440 6 31973120 non coding transcript exon variant A/G snv 7.1E-02 7
rs886424
LINC00243
0.776 0.320 6 30814225 non coding transcript exon variant C/T snv 7.1E-02 8.7E-02 7
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
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
rs3130544 0.807 0.360 6 31090563 intergenic variant C/A snv 7.4E-02 6
rs3131379
MSH5 ; MSH5-SAPCD1
0.752 0.440 6 31753256 intron variant G/A snv 6.4E-02 7.9E-02 6
rs3132580
HCG21 ; SFTA2 ; MUCL3
0.790 0.360 6 30952347 missense variant G/A snv 8.0E-02 9.3E-02 6
rs3134942
NOTCH4
0.790 0.320 6 32200994 synonymous variant G/T snv 9.7E-02 0.11 6
rs558702
C2 ; ZBTB12 ; CYP21A2
0.807 0.320 6 31902549 intron variant G/A snv 7.7E-02 6
rs7762279 0.807 0.360 6 32787513 intergenic variant T/C snv 8.4E-02 6
rs7775397
TSBP1-AS1 ; TSBP1
0.790 0.400 6 32293475 missense variant T/G snv 6.0E-02 6.4E-02 6
rs2523987
TRIM31-AS1 ; TRIM31
0.827 0.280 6 30112216 intron variant A/C snv 9.2E-02 5
rs3094054 0.807 0.280 6 30365728 upstream gene variant G/A;T snv 5
rs3130350 0.827 0.280 6 30360062 upstream gene variant G/T snv 7.1E-02 5
rs3130564
PSORS1C1
0.790 0.360 6 31133897 intron variant C/T snv 0.14 5
rs3132610
ABCF1
0.807 0.280 6 30576624 intron variant A/G snv 7.4E-02 5