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
rs13086367 0.776 0.080 3 113185041 downstream gene variant A/G snv 0.38 10
rs13204733 0.776 0.080 6 55701310 intergenic variant A/G snv 0.10 10
rs13831
GNAS
0.790 0.080 20 58900136 3 prime UTR variant A/G snv 0.77 9
rs141752671 0.708 0.280 11 103745837 intron variant A/G snv 5.4E-03 17
rs142319636
MMP2
0.790 0.080 16 55504828 intron variant A/G snv 3.7E-02 9
rs1453514 0.790 0.080 16 16899146 intergenic variant A/G snv 0.16 9
rs147680653 0.708 0.280 6 29785031 intergenic variant A/G snv 17
rs148883465 0.708 0.280 11 103813371 intron variant A/G snv 7.2E-03 17
rs1535
FADS2
0.752 0.240 11 61830500 intron variant A/G snv 0.31 24
rs16869961
KCNIP4
0.790 0.080 4 20778692 intron variant A/G snv 0.27 9
rs16878812
LOC112267956 ; FKBP5
0.776 0.080 6 35601785 intron variant A/G snv 0.15 10
rs16944613
LOC112268163 ; CRTC3
0.790 0.080 15 90595866 non coding transcript exon variant A/G snv 0.67 9
rs17011141
LINC02257
0.776 0.080 1 221939292 intron variant A/G snv 0.21 10
rs17503919
RNGTT
0.790 0.080 6 88856018 intron variant A/G snv 9.4E-02 10
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs1871438 0.790 0.080 15 92316651 intron variant A/G snv 0.44 9
rs1886450 0.790 0.080 13 73412491 upstream gene variant A/G snv 0.65 9
rs1924816 0.776 0.080 13 73423824 intron variant A/G snv 0.29 10
rs2193352 0.790 0.080 10 99586852 intergenic variant A/G snv 0.15 9
rs2238126
ETV6
0.776 0.080 12 11856807 intron variant A/G snv 0.18 10
rs2286313
PCNX1
0.790 0.080 14 71047446 intron variant A/G snv 4.0E-02 9
rs2730985 0.790 0.080 12 42736822 intergenic variant A/G snv 0.47 9
rs2735940
TERT
0.689 0.400 5 1296371 upstream gene variant A/G snv 0.49 25
rs3131043
HCG20
0.790 0.080 6 30790689 intron variant A/G snv 0.44 9
rs3217901
CCND2
0.790 0.080 12 4296223 intron variant A/G snv 0.35 9