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: rs12410394
rs12410394
0.923 0.071 1 150887710 intron variant G/A snp 0.34
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2011 2011
dbSNP: rs12733285
rs12733285
0.878 0.107 1 202952912 intron variant C/T snp 0.24
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 < 0.001 1 2016 2016
dbSNP: rs13306035
rs13306035
0.923 0.071 1 186672715 3 prime UTR variant A/G snp
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2010 2010
dbSNP: rs138551214
rs138551214
0.923 0.071 1 22909025 missense variant G/A snp 4.0E-06
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2008 2008
dbSNP: rs143353451
rs143353451
0.846 0.107 1 45332794 missense variant C/A,T snp 4.0E-06; 4.0E-06; 1.2E-05 6.4E-05
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2005 2005
dbSNP: rs1476413
rs1476413
0.846 0.143 1 11792243 intron variant C/T snp 4.0E-06; 0.26 0.23
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2014 2014
dbSNP: rs17350795
rs17350795
0.923 0.071 1 13779144 missense variant G/A snp 2.8E-02 1.3E-02
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2016 2016
dbSNP: rs1800872
rs1800872
0.608 0.643 1 206773062 regulatory region variant T/G snp 0.69
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2014 2014
dbSNP: rs1800890
rs1800890
0.724 0.250 1 206776020 intergenic variant A/T snp 0.32
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2010 2010
dbSNP: rs200890679
rs200890679
0.846 0.107 1 11795191 missense variant C/G snp 1.8E-04 2.2E-04
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2015 2015
dbSNP: rs20417
rs20417
0.642 0.393 1 186681189 non coding transcript exon variant C/G,T snp 0.19
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2010 2010
dbSNP: rs20426
rs20426
0.923 0.071 1 186680288 start lost C/T snp
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2010 2010
dbSNP: rs2147578
rs2147578
0.923 0.071 1 183138564 non coding transcript exon variant G/A,C snp 0.53
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2017 2017
dbSNP: rs2297595
rs2297595
0.923 0.071 1 97699535 missense variant T/C snp 8.5E-02 9.0E-02
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2016 2016
dbSNP: rs2760501
rs2760501
0.923 0.071 1 58785425 intron variant T/G snp 0.27
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2011 2011
dbSNP: rs34296044
rs34296044
0.923 0.071 1 241885371 frameshift variant AC/A in-del
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2005 2005
dbSNP: rs35829419
rs35829419
0.801 0.250 1 247425556 missense variant C/A snp 3.9E-02 3.3E-02
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2013 2013
dbSNP: rs377655174
rs377655174
0.923 0.071 1 186678374 missense variant G/A snp 8.1E-06
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2012 2012
dbSNP: rs4131826
rs4131826
0.923 0.071 1 161312594 intergenic variant T/C snp 0.26
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2016 2016
dbSNP: rs4149963
rs4149963
0.923 0.071 1 241872080 missense variant C/T snp 0.11; 6.8E-05 7.5E-02
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2005 2005
dbSNP: rs4646999
rs4646999
0.923 0.071 1 58784780 regulatory region variant A/G snp 0.57
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2011 2011
dbSNP: rs4648298
rs4648298
0.846 0.107 1 186672550 3 prime UTR variant T/C snp 1.6E-02
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2010 2010
dbSNP: rs4659744
rs4659744
MTR
0.923 0.071 1 236896158 intron variant G/C snp 0.36
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2010 2010
dbSNP: rs4846048
rs4846048
0.846 0.107 1 11786195 3 prime UTR variant G/A snp 0.69
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2016 2016
dbSNP: rs4950928
rs4950928
0.679 0.464 1 203186754 regulatory region variant G/A,C,T snp 0.75
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2017 2017