Disease: Adenocarcinoma
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1052133
OGG1 ; CAMK1
0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1048943
CYP1A1
0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 88
rs121434568
EGFR
0.568 0.560 7 55191822 missense variant T/A;G snv 73
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
rs121913530
KRAS
0.583 0.640 12 25245351 missense variant C/A;G;T snv 63
rs121434592
AKT1
0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs121913355
BRAF
0.641 0.520 7 140781602 missense variant C/A;G;T snv 4.0E-06 42
rs401681
CLPTM1L
0.620 0.640 5 1321972 intron variant C/T snv 0.48 42
rs28934575
TP53
0.641 0.400 17 7674230 missense variant C/A;G;T snv 37
rs17851045
KRAS
0.672 0.400 12 25227341 missense variant T/A;G snv 4.0E-06 27
rs121918464
PTPN11
0.708 0.440 12 112450406 missense variant G/A;C snv 25
rs876658657
MLH1
0.677 0.280 3 37020356 missense variant A/G snv 4.0E-06 25
rs121913444
EGFR
0.724 0.160 7 55191831 missense variant T/A;C;G snv 18
rs967461896
TP53
0.724 0.240 17 7675086 missense variant A/C;G;T snv 17
rs587782289
TP53
0.752 0.240 17 7674257 missense variant A/C;G;T snv 15
rs121913465
EGFR ; EGFR-AS1
0.763 0.160 7 55181312 missense variant G/T snv 11
rs2835267
SETD4 ; LOC100133286
0.827 0.080 21 36074727 intron variant T/C snv 0.63 6
rs1367644026
KRT5
0.925 0.080 12 52520259 missense variant C/A;T snv 4.0E-06 5
rs3787728
LOC100133286 ; CBR1 ; SETD4
0.851 0.080 21 36071595 intron variant T/C snv 0.74 5