Disease: Colorectal Carcinoma
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1048945
APEX1 ; OSGEP
0.851 0.120 14 20456008 missense variant G/C snv 2.1E-02 2.4E-02 6
rs12548629
BAALC ; BAALC-AS1
0.776 0.120 8 103189173 intron variant C/T snv 0.24 10
rs1302103336
CHEK1
0.776 0.120 11 125637491 missense variant T/C snv 8.1E-06 12
rs16847024
GC
0.882 0.120 4 71784962 intron variant C/T snv 3.2E-02 4
rs1800056
ATM
0.882 0.120 11 108267276 missense variant T/C snv 8.7E-03 8.5E-03 6
rs1989969
VDR
0.827 0.120 12 47884227 intron variant A/C;G;T snv 0.60 8
rs1990172
MACC1
0.827 0.120 7 20164512 intron variant A/C snv 0.27 6
rs2069522
CYP1A2
0.882 0.120 15 74746892 upstream gene variant T/C snv 5.5E-02 3
rs2302615
ODC1-DT ; SNORA80B ; ODC1
0.807 0.120 2 10448012 intron variant C/T snv 0.31 7
rs3218408
XRCC2
0.882 0.120 7 152670531 intron variant A/C;T snv 3
rs3735684
C7orf50 ; CYP2W1
0.851 0.120 7 985219 missense variant G/A snv 6.8E-02 7.3E-02 4
rs3796508
TLR6 ; TLR1
0.827 0.120 4 38828495 missense variant C/T snv 1.2E-02 1.2E-02 6
rs401618
HLA-A
0.827 0.120 6 29982433 downstream gene variant A/G;T snv 5
rs462779
MFSD4B ; REV3L
0.851 0.120 6 111374684 missense variant G/A snv 0.72 0.67 4
rs4648298
PTGS2
0.882 0.120 1 186672550 3 prime UTR variant T/C snv 1.7E-02 3
rs61753793
FBXO11 ; MSH6
0.851 0.120 2 47799002 missense variant T/C snv 3.6E-05 5.6E-05 4
rs6583267 0.882 0.120 3 195932298 intron variant A/G snv 3
rs6964587
AKAP9
0.851 0.120 7 92001306 missense variant G/T snv 0.38 0.42 4
rs7198799
CDH1
0.882 0.120 16 68784487 intron variant C/T snv 0.27 3
rs749507057
LOC401463 ; BHLHE22
0.851 0.120 8 64580966 missense variant C/T snv 4
rs749539903
ERBB2 ; MIR4728
0.827 0.120 17 39726987 missense variant G/A snv 8.4E-06 9
rs7794030 0.776 0.120 7 38712494 intergenic variant A/G snv 0.23 10
rs8100241
USHBP1 ; ANKLE1
0.827 0.120 19 17282085 missense variant G/A snv 0.47 0.47 5
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