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
rs10505477
CASC8 ; PCAT1 ; POU5F1B
0.658 0.400 8 127395198 intron variant A/G snv 0.40 31
rs1057519847
EGFR
0.570 0.560 7 55191821 missense variant CT/AG mnv 72
rs1057519848
EGFR
0.570 0.560 7 55191822 missense variant TG/GT mnv 72
rs10937405
TP63
0.807 0.080 3 189665394 intron variant C/T snv 0.38 9
rs11134527
MIR218-2 ; SLIT3
0.677 0.400 5 168768351 intron variant G/A snv 0.25 24
rs112445441
KRAS
0.658 0.400 12 25245347 missense variant C/A;G;T snv 32
rs11466345
TGFB1
1.000 0.080 19 41337556 intron variant T/C snv 0.12 2
rs11568820
VDR
0.672 0.480 12 47908762 intron variant C/T snv 0.38 27
rs11991621 1.000 0.080 8 9549072 intergenic variant C/T snv 0.18 2
rs121434568
EGFR
0.568 0.560 7 55191822 missense variant T/A;G snv 73
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs121913444
EGFR
0.724 0.160 7 55191831 missense variant T/A;C;G snv 18
rs121913465
EGFR ; EGFR-AS1
0.763 0.160 7 55181312 missense variant G/T snv 11
rs121913530
KRAS
0.583 0.640 12 25245351 missense variant C/A;G;T snv 63
rs12296850 0.925 0.080 12 100426307 downstream gene variant A/G snv 8.7E-02 3
rs12541709
TNKS
1.000 0.080 8 9751081 intron variant C/G snv 0.29 2
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
rs2564978
CD55
0.827 0.080 1 207321071 upstream gene variant T/C snv 0.77 6
rs2736100
TERT
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs2835267
SETD4 ; LOC100133286
0.827 0.080 21 36074727 intron variant T/C snv 0.63 6
rs2853669
TERT
0.649 0.320 5 1295234 upstream gene variant A/G snv 0.25 35
rs2853677
TERT
0.724 0.240 5 1287079 3 prime UTR variant G/A snv 0.63 19