Disease: Colorectal Carcinoma
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10505477
CASC8 ; PCAT1 ; POU5F1B
0.658 0.400 8 127395198 intron variant A/G snv 0.40 31
rs10680577
RAB4B-EGLN2 ; EGLN2
0.776 0.160 19 40798690 intron variant -/TACT delins 10
rs115797771
KLF5
0.807 0.080 13 73064505 intron variant A/C snv 5.8E-02 6
rs12255372
TCF7L2
0.667 0.480 10 113049143 intron variant G/A;T snv 28
rs12733285
ADIPOR1
0.776 0.120 1 202952912 intron variant C/T snv 0.26 12
rs1342387
ADIPOR1
0.776 0.120 1 202945228 intron variant T/C snv 0.53 12
rs1447295
CASC8
0.658 0.400 8 127472793 intron variant A/C;T snv 29
rs1562430
PCAT1 ; CASC8 ; CASC21 ; POU5F1B
0.807 0.160 8 127375606 intron variant T/C snv 0.41 6
rs1665650
HSPA12A
0.752 0.160 10 116727589 intron variant T/C snv 0.69 12
rs17109928
NOC3L
0.882 0.080 10 94338336 intron variant T/C;G snv 0.15 3
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1800896
IL19 ; IL10
0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1927911
TLR4
0.658 0.640 9 117707776 intron variant A/G snv 0.62 28
rs2057314
DCBLD1
0.882 0.080 6 117498194 intron variant A/G snv 0.61 3
rs2094258
ERCC5 ; BIVM-ERCC5
0.701 0.280 13 102844409 intron variant C/T snv 0.18 20
rs2279744
MDM2
0.605 0.640 12 68808800 intron variant T/G snv 0.31 48
rs2298881
ERCC1
0.653 0.400 19 45423658 intron variant C/A;T snv 25
rs2424913
DNMT3B
0.708 0.440 20 32786453 intron variant C/T snv 0.56 0.53 18
rs28360071
XRCC4
0.708 0.240 5 83142293 intron variant GATGAGGAAACTAACTCTCAGTGGTGTTTA/- delins 0.48 18
rs3781264
PLCE1
0.851 0.120 10 94310618 intron variant A/G snv 0.25 5
rs4778889
IL16
0.683 0.480 15 81296654 intron variant T/C snv 0.24 24
rs4938723
MIR34C ; BTG4 ; MIR34B ; LOC728196
0.574 0.680 11 111511840 intron variant T/C snv 0.32 60
rs4998557
SOD1
0.851 0.080 21 31662579 intron variant G/A snv 0.22 4
rs753724
PLCE1
0.882 0.080 10 94291660 intron variant G/A;C;T snv 4