Disease: Colorectal Carcinoma
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519739
SMAD4
1.000 0.080 18 51065518 missense variant G/A;C snv 2
rs121913327
APC
0.925 0.120 5 112839606 stop gained C/G;T snv 3
rs370662884
CTNNB1
0.925 0.080 3 41225816 synonymous variant G/A snv 3.2E-05 4.9E-05 3
rs138551214
EPHB2
0.925 0.080 1 22909025 missense variant G/A snv 4.0E-06 1.4E-05 4
rs10808555
PCAT1 ; POU5F1B ; CASC8
0.925 0.080 8 127397266 intron variant G/A snv 0.65 6
rs719725 0.827 0.080 9 6365683 intergenic variant A/C snv 0.34 7
rs770248150
KRAS
0.807 0.240 12 25225713 missense variant T/A;G snv 4.0E-06 7
rs772110575
PIK3CA
0.807 0.160 3 179198938 missense variant G/A;T snv 4.0E-06 7
rs1057519890
ERBB2
0.807 0.200 17 39723966 missense variant T/A snv 8
rs7837328
CASC8 ; PCAT1 ; POU5F1B
0.882 0.120 8 127410882 intron variant A/G snv 0.52 8
rs10152518 0.790 0.080 15 67884824 intergenic variant G/A;T snv 9
rs1028166
TENM3 ; TENM3-AS1
0.790 0.080 4 181892145 intron variant G/A snv 0.74 9
rs1035209 0.790 0.080 10 99585609 intergenic variant C/T snv 0.15 9
rs10774214
CCND2-AS1
0.790 0.080 12 4259186 intron variant T/C snv 0.54 9
rs10849432
LOC105369625
0.790 0.080 12 6276561 intergenic variant C/T snv 0.84 9
rs10849438 0.790 0.080 12 6302870 intergenic variant T/G snv 1.0E-01 9
rs10904849
CUBN
0.790 0.080 10 16955267 intron variant G/A;T snv 0.25 9
rs10911251
LAMC1
0.790 0.080 1 183112059 intron variant A/C snv 0.37 9
rs10951878 0.790 0.080 7 46887097 downstream gene variant C/A;T snv 9
rs11064437
SPSB2
0.790 0.080 12 6872998 splice acceptor variant C/T snv 9.3E-02 9
rs11169572 0.790 0.080 12 50823107 downstream gene variant T/C snv 0.42 9
rs113569514
SLCO2A1
0.790 0.080 3 134029945 intron variant T/C snv 0.23 9
rs114436839
PLCH1
0.790 0.080 3 155691561 intron variant G/A snv 1.8E-03 9
rs11893063
LOC105373831
0.790 0.080 2 198737201 intron variant G/A snv 0.37 9
rs11927424 0.790 0.080 3 88708681 intergenic variant A/G snv 0.39 9