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
rs11150038
CLEC3A
0.790 0.080 16 78042662 intron variant A/C;G snv 10
rs11168936
TUBA1C
0.708 0.280 12 49251457 intron variant T/A;C snv 17
rs11169552
ATF1
0.776 0.080 12 50761880 upstream gene variant C/T snv 0.23 10
rs11169572 0.790 0.080 12 50823107 downstream gene variant T/C snv 0.42 9
rs11190164 0.776 0.080 10 99591947 intergenic variant A/G snv 0.19 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
rs11200014
FGFR2
0.695 0.280 10 121575416 intron variant G/A;T snv 0.34 19
rs11255841 0.776 0.080 10 8697617 intergenic variant T/A snv 0.25 11
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
rs115392158
HLA-B
0.708 0.280 6 31347004 intron variant A/G snv 17
rs115707823 0.701 0.320 6 30374976 intergenic variant G/A snv 19
rs11610543 0.776 0.080 12 42740389 intergenic variant A/G;T snv 10
rs116353863 0.776 0.080 6 31042408 regulatory region variant T/C snv 2.2E-02 10
rs117079142
LOC112268030 ; UTP23
0.776 0.080 8 116778675 intron variant C/A snv 3.0E-02 10
rs11844632
RAD51B
0.708 0.280 14 68559662 intron variant G/A snv 0.23 17
rs11874392
SMAD7
0.763 0.080 18 48926786 intron variant A/T snv 0.50 11
rs11884596
LOC105373831
0.776 0.080 2 198747683 intron variant T/C snv 0.32 10
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
rs11907546 0.708 0.280 20 34131991 upstream gene variant C/A;T snv 17
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
rs12144319
TTC22
0.776 0.080 1 54780362 3 prime UTR variant T/C snv 0.31 10