Disease: Colorectal Carcinoma
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2069522
CYP1A2
0.882 0.120 15 74746892 upstream gene variant T/C snv 5.5E-02 3
rs3218408
XRCC2
0.882 0.120 7 152670531 intron variant A/C;T snv 3
rs4648298
PTGS2
0.882 0.120 1 186672550 3 prime UTR variant T/C snv 1.7E-02 3
rs6583267 0.882 0.120 3 195932298 intron variant A/G snv 3
rs7198799
CDH1
0.882 0.120 16 68784487 intron variant C/T snv 0.27 3
rs11014002
MIR603 ; KIAA1217
0.851 0.200 10 24275724 non coding transcript exon variant C/A;T snv 4.1E-06; 7.3E-02 4
rs16847024
GC
0.882 0.120 4 71784962 intron variant C/T snv 3.2E-02 4
rs3735684
C7orf50 ; CYP2W1
0.851 0.120 7 985219 missense variant G/A snv 6.8E-02 7.3E-02 4
rs462779
MFSD4B ; REV3L
0.851 0.120 6 111374684 missense variant G/A snv 0.72 0.67 4
rs61753793
FBXO11 ; MSH6
0.851 0.120 2 47799002 missense variant T/C snv 3.6E-05 5.6E-05 4
rs6964587
AKAP9
0.851 0.120 7 92001306 missense variant G/T snv 0.38 0.42 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
rs2070894
CRYAB
0.851 0.160 11 111910113 3 prime UTR variant G/A snv 0.27 5
rs2228387
CRYAB ; HSPB2-C11orf52 ; HSPB2
0.851 0.160 11 111911560 synonymous variant C/G;T snv 1.5E-02 5
rs2230009
WRN
0.827 0.240 8 31064419 missense variant G/A snv 5.8E-02 7.8E-02 5
rs2289046
IRS2
0.827 0.240 13 109755559 3 prime UTR variant T/C snv 0.27 5
rs401618
HLA-A
0.827 0.120 6 29982433 downstream gene variant A/G;T snv 5
rs7000448
CASC8
0.827 0.160 8 127428925 intron variant C/T snv 0.45 5
rs7336610
MIR17HG
0.827 0.240 13 91352883 intron variant C/T snv 0.47 5
rs8100241
USHBP1 ; ANKLE1
0.827 0.120 19 17282085 missense variant G/A snv 0.47 0.47 5
rs8752
HPGD
0.827 0.160 4 174491326 3 prime UTR variant C/T snv 0.49 5
rs9383938
ESR1
0.827 0.160 6 151666222 intron variant G/T snv 0.11 5
rs10380
MTRR
0.807 0.200 5 7897078 missense variant C/T snv 0.16 0.18 6