Disease: Malignant tumor of colon
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
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
rs11692435
ACTR1B
0.790 0.080 2 97658891 missense variant G/A snv 7.0E-02 6.7E-02 10
rs117079142
LOC112268030 ; UTP23
0.776 0.080 8 116778675 intron variant C/A snv 3.0E-02 10
rs11727676
HHIP
0.776 0.080 4 144737912 synonymous variant T/C snv 6.6E-02 6.4E-02 14
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
rs11927424 0.790 0.080 3 88708681 intergenic variant A/G snv 0.39 9
rs119490107
FSBP ; RAD54B
0.925 0.080 8 94399540 missense variant C/A snv 2.8E-05 2
rs11986055
IKBKB
0.882 0.080 8 42277660 intron variant A/C;G snv 3
rs121434507
PTPRJ
0.925 0.080 11 48123636 missense variant C/T snv 4.0E-05 6.3E-05 2
rs121434623
PTPN12
0.925 0.080 7 77571160 missense variant A/G snv 2
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
rs12149163 0.776 0.080 16 86305709 upstream gene variant T/C snv 0.49 10
rs121909242
PPARG
0.925 0.080 3 12416825 missense variant A/C snv 2
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
rs12372718
ATF1
0.776 0.080 12 50777307 intron variant A/G snv 0.35 10
rs12412391
LINC01475
0.790 0.080 10 99529178 intron variant A/G;T snv 9
rs12427600
SMAD9
0.790 0.080 13 36886511 intron variant T/C snv 0.23 9