Disease: Malignant neoplasm of large intestine
Source: GWASCAT ×
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
rs10411210
RHPN2
0.742 0.160 19 33041394 intron variant C/T snv 0.22 9
rs10506868
VTI1A
0.716 0.160 10 112559621 intron variant C/T snv 3.1E-02 9
rs10774214
CCND2-AS1
0.790 0.080 12 4259186 intron variant T/C snv 0.54 9
rs10795668
LOC105376400
0.724 0.160 10 8659256 upstream gene variant G/A snv 0.24 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
rs11169552
ATF1
0.776 0.080 12 50761880 upstream gene variant C/T snv 0.23 9
rs11169572 0.790 0.080 12 50823107 downstream gene variant T/C snv 0.42 9
rs11196172
TCF7L2
0.708 0.200 10 112967084 intron variant G/A snv 0.13 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
rs11903757 0.763 0.160 2 191722478 intron variant T/C snv 0.16 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
rs12241008
VTI1A
0.716 0.160 10 112520943 intron variant T/C snv 0.13 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