Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs12143541
TTC22
0.790 0.080 1 54782179 intron variant A/G snv 0.11 9
rs12255141
VTI1A
0.790 0.080 10 112535133 intron variant A/G;T snv 9
rs12412391
LINC01475
0.790 0.080 10 99529178 intron variant A/G;T snv 9
rs12427600
SMAD9
0.790 0.080 13 36886511 intron variant T/C snv 0.23 9
rs12603526
NXN
0.790 0.080 17 897353 intron variant T/C snv 2.3E-02 9
rs12635946 0.790 0.080 3 113198071 intergenic variant C/T snv 0.32 9
rs12659017 0.790 0.080 5 126652483 intergenic variant G/A snv 0.27 9
rs12682374
POU5F1B ; PCAT1 ; CCAT2 ; CASC8
0.790 0.080 8 127398703 intron variant C/A;G;T snv 9
rs12818766
CCND2-AS1
0.790 0.080 12 4266925 intron variant G/A snv 0.17 9
rs12979278
MAMSTR
0.790 0.080 19 48715345 synonymous variant C/T snv 0.46 0.40 9