Disease: Adenocarcinoma
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10503380 1.000 0.080 8 9552985 upstream gene variant C/T snv 0.25 2
rs11466345
TGFB1
1.000 0.080 19 41337556 intron variant T/C snv 0.12 2
rs11991621 1.000 0.080 8 9549072 intergenic variant C/T snv 0.18 2
rs12541709
TNKS
1.000 0.080 8 9751081 intron variant C/G snv 0.29 2
rs586339
KDM4A
1.000 0.080 1 43671586 missense variant C/A;G;T snv 0.70 0.78 2
rs6601328 1.000 0.080 8 9545693 regulatory region variant G/A;C snv 2
rs7015700
TNKS
1.000 0.080 8 9670197 splice donor variant G/A snv 0.23 2
rs12296850 0.925 0.080 12 100426307 downstream gene variant A/G snv 8.7E-02 3
rs1340420
TNKS2
0.925 0.080 10 91857549 intron variant A/G snv 0.71 0.70 3
rs1770474
TNKS2
0.925 0.080 10 91833770 intron variant G/A;T snv 3
rs181696
PLCH1
0.925 0.080 3 155548315 intron variant T/C snv 0.55 3
rs2269577
XBP1 ; ZNRF3
0.882 0.120 22 28800769 non coding transcript exon variant G/C snv 0.40 4
rs1367644026
KRT5
0.925 0.080 12 52520259 missense variant C/A;T snv 4.0E-06 5
rs3114020
ABCG2
0.882 0.200 4 88162514 intron variant T/C snv 0.40 5
rs3787728
LOC100133286 ; CBR1 ; SETD4
0.851 0.080 21 36071595 intron variant T/C snv 0.74 5
rs759435862
KIDINS220
0.925 0.080 2 8776852 missense variant C/A;T snv 2.0E-05 5
rs2564978
CD55
0.827 0.080 1 207321071 upstream gene variant T/C snv 0.77 6
rs2835267
SETD4 ; LOC100133286
0.827 0.080 21 36074727 intron variant T/C snv 0.63 6
rs3660
KRT86 ; KRT81
0.882 0.160 12 52286153 3 prime UTR variant C/G snv 0.51 6
rs689465
PTGS2 ; PACERR
0.851 0.200 1 186681714 upstream gene variant T/C snv 0.14 7
rs2279574
DUSP6
0.827 0.120 12 89351700 missense variant C/A;T snv 0.52 8
rs10937405
TP63
0.807 0.080 3 189665394 intron variant C/T snv 0.38 9
rs28929495
EGFR
0.807 0.120 7 55174014 missense variant G/A;C;T snv 9
rs397517108
EGFR ; EGFR-AS1
0.790 0.120 7 55181312 missense variant GC/TT mnv 9
rs33917957
MET
0.790 0.120 7 116700208 missense variant A/G snv 2.7E-02 1.8E-02 10