Source: BEFREE

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: rs997476
rs997476
0.882 0.080 4 102620848 downstream gene variant G/T snv 4.3E-02
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2013 2013
dbSNP: rs995343
rs995343
0.925 0.120 12 59685594 intron variant G/A snv 0.57
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2015 2015
dbSNP: rs9944880
rs9944880
DCC
0.882 0.120 18 53125996 intron variant G/A snv 5.3E-02
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2018 2018
dbSNP: rs9939609
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2012 2012
dbSNP: rs9939049
rs9939049
0.790 0.080 16 68778398 intron variant A/T snv 0.29
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.710 1.000 1 2019 2020
dbSNP: rs9929218
rs9929218
0.732 0.160 16 68787043 intron variant G/A snv 0.28
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.850 1.000 5 2008 2016
dbSNP: rs992157
rs992157
0.790 0.080 2 218290058 5 prime UTR variant G/A snv 0.46
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.730 1.000 3 2016 2019
dbSNP: rs9921222
rs9921222
0.925 0.120 16 325782 intron variant C/T snv 0.51
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2019 2019
dbSNP: rs9912300
rs9912300
0.827 0.120 17 41869011 intron variant G/A;C;T snv 4.2E-06; 0.78
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2015 2015
dbSNP: rs9904341
rs9904341
0.695 0.280 17 78214286 5 prime UTR variant G/A;C;T snv 0.38; 4.8E-06
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2014 2014
dbSNP: rs989902
rs989902
0.742 0.240 4 86785353 missense variant T/G snv 0.42 0.53
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2017 2017
dbSNP: rs9858822
rs9858822
0.925 0.080 3 12369739 intron variant A/C snv 0.11
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2013 2013
dbSNP: rs984907158
rs984907158
0.925 0.080 2 47799048 synonymous variant T/C snv 4.0E-06 2.8E-05
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2007 2007
dbSNP: rs982873
rs982873
0.925 0.160 13 90145678 intergenic variant T/C snv 0.65
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2017 2017
dbSNP: rs980578884
rs980578884
0.925 0.080 12 132673217 missense variant C/T snv 1.4E-05
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2017 2017
dbSNP: rs979090956
rs979090956
0.827 0.200 7 87553822 missense variant G/C snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2015 2015
dbSNP: rs9651118
rs9651118
0.683 0.480 1 11802157 intron variant T/C snv 0.18
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2017 2017
dbSNP: rs964293
rs964293
0.790 0.080 20 54200178 TF binding site variant C/A;T snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.710 1.000 1 2016 2016
dbSNP: rs9620817
rs9620817
0.851 0.120 22 28712568 intron variant A/T snv 8.4E-02
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2018 2018
dbSNP: rs961253
rs961253
0.732 0.240 20 6423634 intergenic variant C/A snv 0.34
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.860 1.000 6 2008 2019
dbSNP: rs9588884
rs9588884
1.000 0.080 13 90145067 intergenic variant C/G snv 0.70
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2017 2017
dbSNP: rs9513070
rs9513070
0.851 0.080 13 28305702 intron variant G/A snv 0.54
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2014 2014
dbSNP: rs9502893
rs9502893
0.827 0.120 6 1339954 intergenic variant C/G;T snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2016 2016
dbSNP: rs941759532
rs941759532
0.763 0.240 16 13932175 missense variant C/G snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2006 2006
dbSNP: rs9383938
rs9383938
0.827 0.160 6 151666222 intron variant G/T snv 0.11
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2019 2019