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
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
rs10506868
VTI1A
0.716 0.160 10 112559621 intron variant C/T snv 3.1E-02 16
rs755229494
APC
0.776 0.080 5 112761654 intron variant A/G snv 9.6E-04 10
rs11196170
TCF7L2
0.776 0.080 10 112962862 intron variant G/A;C snv 10
rs11196172
TCF7L2
0.708 0.200 10 112967084 intron variant G/A snv 0.13 18
rs13086367 0.776 0.080 3 113185041 downstream gene variant A/G snv 0.38 10
rs12635946 0.790 0.080 3 113198071 intergenic variant C/T snv 0.32 9
rs72942485
BOC
0.776 0.080 3 113280713 intron variant G/A snv 2.7E-02 4.5E-02 10
rs16845107
CFAP44 ; CFAP44-AS1
0.790 0.080 3 113409144 missense variant C/A snv 7.2E-02 7.4E-02 9
rs10511330
ZBTB20
0.776 0.080 3 114402172 intron variant T/C snv 0.22 10
rs1427760 0.776 0.080 12 114662909 upstream gene variant T/C snv 0.49 10
rs59336
TBX3
0.776 0.160 12 114678547 intron variant T/A;G snv 0.49 10
rs7300312
LOC105370003
0.776 0.080 12 115453117 intergenic variant T/C snv 0.61 10
rs7315438
LOC105370003
0.790 0.080 12 115453598 intergenic variant C/A;T snv 9
rs4378954
LSAMP
0.790 0.080 3 115931601 intron variant T/C snv 0.83 10
rs140355816 0.790 0.080 8 116562277 intergenic variant C/G snv 9.8E-03 9
rs2450115
LOC105375712
0.790 0.080 8 116611854 intergenic variant T/C snv 0.19 9
rs3133285 0.776 0.080 8 116617172 intergenic variant G/C snv 0.19 10
rs16892766 0.716 0.240 8 116618444 intergenic variant A/C snv 9.3E-02 18
rs6469654 0.776 0.080 8 116620726 intergenic variant G/C snv 0.64 10
rs6469656 0.790 0.080 8 116635549 regulatory region variant G/A;C snv 9
rs1665650
HSPA12A
0.752 0.160 10 116727589 intron variant T/C snv 0.69 12
rs117079142
LOC112268030 ; UTP23
0.776 0.080 8 116778675 intron variant C/A snv 3.0E-02 10
rs76316943
UTP23
0.790 0.080 8 116836068 intron variant G/A snv 1.3E-02 9