Disease: Colorectal Carcinoma
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519925
PIK3CA
0.683 0.560 3 179210291 missense variant G/A;C snv 25
rs6505162
NSRP1 ; MIR3184 ; MIR423
0.695 0.320 17 30117165 5 prime UTR variant A/C;T snv 0.50; 3.1E-05 25
rs138213197
HOXB13
0.701 0.240 17 48728343 missense variant C/T snv 1.8E-03 1.6E-03 24
rs121913286
PIK3CA
0.677 0.280 3 179218306 missense variant C/A;G snv 23
rs121913348
BRAF
0.763 0.480 7 140781617 missense variant C/A;G;T snv 20
rs1057519895
FBXW7
0.724 0.240 4 152328232 missense variant C/A;G;T snv 17
rs121913283
PIK3CA
0.724 0.440 3 179234286 missense variant G/A;T snv 4.0E-06 16
rs56391007
MET
0.752 0.200 7 116771936 missense variant C/T snv 7.9E-03 9.0E-03 16
rs587780071
TP53
0.732 0.240 17 7674951 missense variant G/A snv 15
rs377767347
SMAD4
0.742 0.520 18 51065549 missense variant G/A;C;T snv 14
rs121913272
PIK3CA
0.752 0.400 3 179210192 missense variant T/C;G snv 13
rs1302103336
CHEK1
0.776 0.120 11 125637491 missense variant T/C snv 8.1E-06 12
rs1057519738
MIR4728 ; ERBB2
0.790 0.160 17 39725079 missense variant G/A snv 4.0E-06 10
rs1057519943
POLE
0.790 0.160 12 132676598 missense variant G/C;T snv 10
rs1057519890
ERBB2
0.807 0.200 17 39723966 missense variant T/A snv 8