Disease: Malignant neoplasm of colon and/or rectum
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3763511
DKK4
0.882 0.120 8 42378340 upstream gene variant G/A snv 0.24 3
rs3735684
C7orf50 ; CYP2W1
0.851 0.120 7 985219 missense variant G/A snv 6.8E-02 7.3E-02 4
rs749507057
LOC401463 ; BHLHE22
0.851 0.120 8 64580966 missense variant C/T snv 4
rs932335
HSD11B1-AS1 ; HSD11B1
0.851 0.120 1 209732389 intron variant G/C snv 0.21 0.21 4
rs9620817
CHEK2
0.851 0.120 22 28712568 intron variant A/T snv 8.4E-02 4
rs401618
HLA-A
0.827 0.120 6 29982433 downstream gene variant A/G;T snv 5
rs7336610
MIR17HG
0.827 0.240 13 91352883 intron variant C/T snv 0.47 5
rs10380
MTRR
0.807 0.200 5 7897078 missense variant C/T snv 0.16 0.18 6
rs1048945
APEX1 ; OSGEP
0.851 0.120 14 20456008 missense variant G/C snv 2.1E-02 2.4E-02 6
rs1990172
MACC1
0.827 0.120 7 20164512 intron variant A/C snv 0.27 6
rs3796508
TLR6 ; TLR1
0.827 0.120 4 38828495 missense variant C/T snv 1.2E-02 1.2E-02 6
rs796096871
AKAP10
0.807 0.200 17 19909228 missense variant TG/CA mnv 6
rs10090154 0.807 0.160 8 127519892 intergenic variant T/A;C snv 7
rs203462
AKAP10
0.807 0.200 17 19909228 missense variant T/C snv 0.37 0.43 7
rs2302615
ODC1-DT ; SNORA80B ; ODC1
0.807 0.120 2 10448012 intron variant C/T snv 0.31 7
rs8679
PARP1
0.790 0.200 1 226360853 3 prime UTR variant A/G snv 0.16 7
rs6498486
ERCC4
0.776 0.200 16 13919809 upstream gene variant A/C snv 0.27 8
rs11685387
XRCC5
0.776 0.240 2 216109091 splice region variant C/T snv 0.30 9
rs175080
MLH3
0.776 0.240 14 75047125 missense variant G/A snv 0.40 0.43 9
rs26279
MSH3
0.790 0.160 5 80873118 missense variant G/A snv 0.73 0.70 9
rs5277
PACERR ; PTGS2
0.790 0.160 1 186679065 synonymous variant C/G;T snv 0.12; 8.0E-06 9
rs7086803
VTI1A
0.763 0.160 10 112738717 intron variant G/A snv 0.20 9
rs7421861
LOC105373977 ; PDCD1
0.790 0.200 2 241853198 intron variant A/G;T snv 9
rs7539542
ADIPOR1
0.807 0.200 1 202940846 3 prime UTR variant G/C snv 0.58 9
rs7904519
TCF7L2
0.763 0.240 10 113014168 intron variant A/G snv 0.55 9