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
rs11893063
LOC105373831
0.790 0.080 2 198737201 intron variant G/A snv 0.37 9
rs11903757 0.763 0.160 2 191722478 intron variant T/C snv 0.16 11
rs13020391
LOC105373881 ; PNKD
0.790 0.080 2 218319713 intron variant C/T snv 0.32 9
rs1367374 0.790 0.080 2 153074663 intergenic variant G/C snv 0.19 9
rs2901879 0.790 0.080 2 66738934 intergenic variant C/T snv 0.54 9
rs3731861
PNKD ; CATIP-AS2
0.776 0.080 2 218326533 intron variant T/C snv 0.32 10
rs448513
TANC1
0.776 0.080 2 159108040 intron variant T/C snv 0.41 10
rs4849303
ACOXL
0.790 0.080 2 110970905 intron variant C/G;T snv 9
rs4954585 0.790 0.080 2 136240824 intergenic variant C/G;T snv 9
rs6720296
LINC01121
0.790 0.080 2 45181130 intron variant A/C snv 0.52 9
rs7593422 0.790 0.080 2 199266972 downstream gene variant A/T snv 0.41 9
rs7606512
LINC01173
0.790 0.080 2 234701030 intron variant C/T snv 0.11 9
rs7606562
PPP1R21
0.790 0.080 2 48459556 intron variant T/A;C snv 9
rs983402 0.776 0.080 2 198916862 intron variant T/C snv 0.62 10
rs992157
TMBIM1 ; PNKD
0.790 0.080 2 218290058 5 prime UTR variant G/A snv 0.46 10
rs10049390
SLCO2A1
0.776 0.080 3 133982275 intron variant G/A snv 0.67 10
rs10511330
ZBTB20
0.776 0.080 3 114402172 intron variant T/C snv 0.22 10
rs10936599
MYNN
0.637 0.600 3 169774313 synonymous variant C/T snv 0.29 0.21 32
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
rs11927424 0.790 0.080 3 88708681 intergenic variant A/G snv 0.39 9
rs12635946 0.790 0.080 3 113198071 intergenic variant C/T snv 0.32 9
rs13086367 0.776 0.080 3 113185041 downstream gene variant A/G snv 0.38 10
rs16845107
CFAP44 ; CFAP44-AS1
0.790 0.080 3 113409144 missense variant C/A snv 7.2E-02 7.4E-02 9
rs17659990
DOCK3
0.790 0.080 3 50713718 intron variant C/T snv 2.1E-02 9