Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs113488022
rs113488022
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.900 0.975 160 2004 2020
dbSNP: rs1217691063
rs1217691063
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.100 0.829 70 1999 2018
dbSNP: rs6983267
rs6983267
0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.900 0.945 55 2007 2019
dbSNP: rs1801155
rs1801155
APC
0.649 0.440 5 112839514 missense variant T/A snv 8.0E-06; 2.0E-03 1.2E-03
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.800 0.861 36 1997 2017
dbSNP: rs397507444
rs397507444
0.405 0.880 1 11794407 missense variant T/G snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.100 0.806 31 2002 2019
dbSNP: rs4939827
rs4939827
0.708 0.160 18 48927093 intron variant T/A;C snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.900 0.964 28 2007 2019
dbSNP: rs25487
rs25487
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.100 0.833 24 2004 2016
dbSNP: rs3802842
rs3802842
0.695 0.280 11 111300984 intron variant C/A snv 0.71
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.900 1.000 24 2008 2019
dbSNP: rs397517132
rs397517132
0.623 0.280 7 55191846 missense variant A/T snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.100 0.913 23 2008 2019
dbSNP: rs1042522
rs1042522
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.100 0.727 22 2006 2019
dbSNP: rs16892766
rs16892766
0.716 0.240 8 116618444 intergenic variant A/C snv 9.3E-02
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.900 1.000 19 2008 2019
dbSNP: rs1052133
rs1052133
0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.100 0.500 18 2005 2019
dbSNP: rs11614913
rs11614913
0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.100 0.882 17 2011 2018
dbSNP: rs1695
rs1695
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.100 0.882 17 2002 2019
dbSNP: rs2910164
rs2910164
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.100 0.824 17 2012 2018
dbSNP: rs34612342
rs34612342
0.653 0.400 1 45332803 missense variant T/C snv 1.5E-03 1.6E-03
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.800 1.000 17 2002 2019
dbSNP: rs36053993
rs36053993
0.677 0.280 1 45331556 missense variant C/T snv 3.0E-03 3.3E-03
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.800 0.941 17 2002 2019
dbSNP: rs10505477
rs10505477
0.658 0.400 8 127395198 intron variant A/G snv 0.40
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.890 0.938 16 2007 2019
dbSNP: rs10795668
rs10795668
0.724 0.160 10 8659256 upstream gene variant G/A snv 0.24
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.900 1.000 15 2008 2019
dbSNP: rs13181
rs13181
0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.100 0.800 15 2005 2019
dbSNP: rs861539
rs861539
0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.100 0.933 15 2004 2018
dbSNP: rs1045642
rs1045642
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.100 0.929 14 2003 2019
dbSNP: rs121913364
rs121913364
0.641 0.520 7 140753334 missense variant T/C;G snv 4.0E-06
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.800 1.000 14 2002 2015
dbSNP: rs12953717
rs12953717
0.724 0.240 18 48927559 intron variant C/T snv 0.36
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.900 1.000 14 2007 2018
dbSNP: rs1799782
rs1799782
0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.100 0.857 14 2009 2016