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
rs10318
GREM1
0.882 0.080 15 32733778 3 prime UTR variant C/T snv 0.16 3
rs1051424
RPS6KB1
0.925 0.080 17 59946963 3 prime UTR variant A/G snv 0.15 3
rs1051690
INSR
0.851 0.080 19 7116952 3 prime UTR variant T/C snv 0.83 4
rs1052748
PLD2
0.925 0.080 17 4817174 missense variant C/T snv 0.39 0.36 2
rs1057519860
EGFR
0.851 0.080 7 55160316 missense variant C/A snv 5
rs1063169
FOS
0.925 0.080 14 75280415 5 prime UTR variant G/T snv 0.12 2
rs1064795747
MSH2
0.925 0.080 2 47412433 missense variant T/C snv 4
rs1064795841
TP53
0.882 0.080 17 7674971 missense variant C/T snv 4
rs1065411
GSTM2 ; GSTM1
0.925 0.080 1 109690516 missense variant G/A;C;T snv 0.36; 6.9E-06 2
rs10845671
GPRC5D-AS1
0.925 0.080 12 12926708 upstream gene variant C/A;T snv 2
rs10883782
WBP1L
0.925 0.080 10 102824175 intron variant A/G snv 0.14 2
rs1088967 0.851 0.080 X 127010099 intergenic variant T/A;C snv 4
rs11169552
ATF1
0.776 0.080 12 50761880 upstream gene variant C/T snv 0.23 10
rs11568591
ABCC3
0.925 0.080 17 50683692 missense variant G/A snv 3.7E-02 3.9E-02 2
rs115797771
KLF5
0.807 0.080 13 73064505 intron variant A/C snv 5.8E-02 6
rs116896264
LGALS4
0.925 0.080 19 38813176 upstream gene variant G/T snv 9.0E-02 2
rs11704
CINP ; ZNF839
0.925 0.080 14 102342318 3 prime UTR variant G/C snv 0.26 2
rs1176119168
HSPA1B
0.925 0.080 6 31828202 missense variant G/A;T snv 1.9E-05 2
rs118049207
SND1
0.925 0.080 7 127890817 intron variant A/G snv 1.7E-03 2
rs11874392
SMAD7
0.763 0.080 18 48926786 intron variant A/T snv 0.50 11
rs1194338 0.925 0.080 11 65493967 upstream gene variant C/A;T snv 3
rs12037879
LEPR
0.925 0.080 1 65477024 intron variant G/A;T snv 5
rs1215486792
MOK
0.925 0.080 14 102229572 missense variant C/G snv 7.0E-06 2
rs1230416942
TTI2 ; MAK16
0.925 0.080 8 33498547 missense variant G/C snv 7.0E-06 3
rs12373
ZG16B
0.925 0.080 16 2832196 3 prime UTR variant G/T snv 0.66 0.63 2