Disease: Adenocarcinoma
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913355
BRAF
0.641 0.520 7 140781602 missense variant C/A;G;T snv 4.0E-06 42
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs10505477
CASC8 ; PCAT1 ; POU5F1B
0.658 0.400 8 127395198 intron variant A/G snv 0.40 31
rs397517132
EGFR
0.623 0.280 7 55191846 missense variant A/T snv 48
rs1057519816
ERBB2
0.763 0.200 17 39711955 missense variant C/A;T snv 14
rs112445441
KRAS
0.658 0.400 12 25245347 missense variant C/A;G;T snv 32
rs121913529
KRAS
0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144
rs121913530
KRAS
0.583 0.640 12 25245351 missense variant C/A;G;T snv 63
rs17851045
KRAS
0.672 0.400 12 25227341 missense variant T/A;G snv 4.0E-06 27
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs121913237
NRAS
0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 50
rs121918464
PTPN11
0.708 0.440 12 112450406 missense variant G/A;C snv 25
rs1057519747
TP53
0.716 0.280 17 7675094 missense variant A/C;G;T snv 23
rs28934575
TP53
0.641 0.400 17 7674230 missense variant C/A;G;T snv 37
rs587782289
TP53
0.752 0.240 17 7674257 missense variant A/C;G;T snv 15
rs967461896
TP53
0.724 0.240 17 7675086 missense variant A/C;G;T snv 17