Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12149163 0.776 0.080 16 86305709 upstream gene variant T/C snv 0.49 10
rs12241008
VTI1A
0.716 0.160 10 112520943 intron variant T/C snv 0.13 16
rs12246635
VTI1A
0.776 0.080 10 112528860 intron variant T/C snv 0.13 10
rs12255141
VTI1A
0.790 0.080 10 112535133 intron variant A/G;T snv 9
rs12372718
ATF1
0.776 0.080 12 50777307 intron variant A/G snv 0.35 10
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
rs12447408 0.776 0.080 16 86218938 downstream gene variant G/A snv 0.21 10
rs1250567
ZMIZ1
0.776 0.080 10 79286508 intron variant T/C snv 0.56 10
rs12514517 0.776 0.080 5 40279974 intergenic variant G/A snv 0.21 10
rs12548629
BAALC ; BAALC-AS1
0.776 0.120 8 103189173 intron variant C/T snv 0.24 10
rs12594720
SMAD6
0.776 0.080 15 66714680 intron variant C/G snv 0.23 10
rs12601991
HNF1B
0.708 0.280 17 37741642 intron variant T/A;G snv 17
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
rs12646351
ZNF827
0.790 0.080 4 145819473 intron variant G/A snv 0.19 10
rs12659017 0.790 0.080 5 126652483 intergenic variant G/A snv 0.27 9
rs12672022 0.776 0.080 7 45096824 downstream gene variant T/C snv 0.13 10
rs12682374
POU5F1B ; PCAT1 ; CCAT2 ; CASC8
0.790 0.080 8 127398703 intron variant C/A;G;T snv 9
rs12708491 0.776 0.080 15 32700635 downstream gene variant G/A snv 0.33 10
rs12818766
CCND2-AS1
0.790 0.080 12 4266925 intron variant G/A snv 0.17 9
rs12916300
HERC2
0.742 0.080 15 28165345 intron variant C/T snv 0.50 13
rs12953717
SMAD7
0.724 0.240 18 48927559 intron variant C/T snv 0.36 18
rs12970291 0.763 0.120 18 75305279 intergenic variant G/A snv 2.8E-02 12
rs13020391
LOC105373881 ; PNKD
0.790 0.080 2 218319713 intron variant C/T snv 0.32 9