Disease: Carcinoma of lung
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10889677
IL23R
0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 40
rs11137037
ANGPT2 ; MCPH1
0.851 0.200 8 6538661 intron variant A/C snv 0.40 4
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs11543848
EGFR
0.790 0.240 7 55161562 missense variant G/A;C;T snv 7
rs1222213359
VEGFA
0.574 0.720 6 43770966 missense variant G/A snv 62
rs12674822
MCPH1 ; ANGPT2
0.851 0.200 8 6531695 intron variant T/G snv 0.49 4
rs12826786 0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38 26
rs12901682
PSMA4
0.851 0.200 15 78540881 5 prime UTR variant A/C;T snv 4
rs1360485
HMGB1
0.742 0.320 13 30457747 3 prime UTR variant C/T snv 0.58 16
rs1412125
HMGB1
0.724 0.360 13 30467458 intron variant C/G;T snv 17
rs1535045
CD40
0.742 0.360 20 46119460 intron variant C/A;G;T snv 12
rs1799724
LTA ; TNF
0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02 47
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs1800625
AGER ; PBX2
0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 39
rs1800796
IL6-AS1 ; STEAP1B ; IL6
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 74
rs1800871
IL19 ; IL10
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs1800872
IL19 ; IL10
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs1800896
IL19 ; IL10
0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs2075786
TERT
0.790 0.360 5 1266195 intron variant A/G snv 0.55 8
rs2243250
IL4
0.570 0.760 5 132673462 upstream gene variant C/T snv 0.35 61
rs2249825
HMGB1
0.695 0.440 13 30463766 5 prime UTR variant G/A;C;T snv 23
rs2275913
IL17A
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs2281089
IL2RB
0.851 0.200 22 37136132 intron variant A/G snv 0.17 4
rs2395185
HLA-DRB9
0.724 0.360 6 32465390 intron variant G/T snv 0.29 17
rs28362491
LOC105377621 ; NFKB1
0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 56