Disease: Malignant neoplasm of lung
Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7086803
VTI1A
0.763 0.160 10 112738717 intron variant G/A snv 0.20 4
rs9387478
DCBLD1
0.851 0.080 6 117465017 intron variant C/A;T snv 3
rs2736100
TERT
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 16
rs4635969 0.827 0.160 5 1308437 downstream gene variant G/A;T snv 5
rs4975616 0.763 0.320 5 1315545 downstream gene variant G/A snv 0.51 5
rs401681
CLPTM1L
0.620 0.640 5 1321972 intron variant C/T snv 0.48 17
rs31489
CLPTM1L
0.763 0.320 5 1342599 intron variant C/A snv 0.41 5
rs13314271
TP63
0.925 0.080 3 189639813 intron variant T/C snv 0.45 2
rs4324798 0.790 0.240 6 28808340 intergenic variant G/A snv 7.2E-02 5
rs3129791
HCG15
0.827 0.280 6 28986516 intron variant G/A snv 5.3E-02 5
rs3130893 0.882 0.160 6 29012930 intergenic variant A/G snv 5.3E-02 3
rs3117143
LOC100129636
0.882 0.160 6 29063365 intron variant C/A snv 5.2E-02 4
rs2746150 0.851 0.240 6 29474924 downstream gene variant C/T snv 5.3E-02 4
rs1235162
GABBR1
0.827 0.280 6 29569447 intron variant A/G snv 6.0E-02 6
rs2734986
LOC105375010
0.827 0.160 6 29850791 intron variant T/C snv 0.10 3
rs2256543
HLA-A
0.925 0.080 6 29970056 downstream gene variant T/C snv 0.59 2
rs3132685
HLA-A ; HCG9
0.807 0.320 6 29978172 intron variant G/A;T snv 6
rs259940
ZNRD1ASP
0.925 0.080 6 30044157 intron variant A/G snv 0.23 2
rs259919
ZNRD1ASP
0.882 0.080 6 30057726 intron variant G/A snv 0.25 6
rs8321
ZNRD1
0.742 0.320 6 30064745 3 prime UTR variant A/C snv 5.4E-02 5.9E-02 15
rs9261290
RNF39
0.807 0.280 6 30070870 3 prime UTR variant T/C;G snv 5.2E-02; 7.2E-06 10
rs2523987
TRIM31-AS1 ; TRIM31
0.827 0.280 6 30112216 intron variant A/C snv 9.2E-02 5
rs3130380
HCG18 ; HCG17
0.807 0.280 6 30311353 intron variant G/A snv 6.6E-02 10
rs3130350 0.827 0.280 6 30360062 upstream gene variant G/T snv 7.1E-02 5
rs3094054 0.807 0.280 6 30365728 upstream gene variant G/A;T snv 6