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: rs3774959
rs3774959
0.925 0.080 4 102589957 intron variant G/A snv 0.34
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2012 2012
dbSNP: rs3774964
rs3774964
1.000 0.080 4 102598330 intron variant A/G snv 0.39
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2012 2012
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: rs770635391
rs770635391
1.000 0.080 19 10271190 missense variant C/G;T snv 8.1E-06; 4.1E-06
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2006 2006
dbSNP: rs750521832
rs750521832
0.732 0.200 11 102718452 missense variant A/G snv 4.0E-06
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2015 2015
dbSNP: rs10883782
rs10883782
0.925 0.080 10 102824175 intron variant A/G snv 0.14
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2011 2011
dbSNP: rs4919687
rs4919687
0.742 0.160 10 102835491 non coding transcript exon variant G/A snv 0.25
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.710 1.000 1 2016 2016
dbSNP: rs1799969
rs1799969
0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.020 1.000 2 2006 2009
dbSNP: rs2094258
rs2094258
0.701 0.280 13 102844409 intron variant C/T snv 0.18
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2016 2016
dbSNP: rs17724534
rs17724534
0.925 0.080 10 102845764 non coding transcript exon variant C/T snv 9.1E-02
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2011 2011
dbSNP: rs751402
rs751402
0.724 0.360 13 102845848 5 prime UTR variant A/G snv 0.76
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2016 2016
dbSNP: rs2296147
rs2296147
0.695 0.280 13 102846025 5 prime UTR variant T/C snv 0.38
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2016 2016
dbSNP: rs5498
rs5498
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.030 1.000 3 2006 2017
dbSNP: rs2276109
rs2276109
0.701 0.440 11 102875061 upstream gene variant T/C snv 9.2E-02
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2013 2013
dbSNP: rs17655
rs17655
0.597 0.560 13 102875652 missense variant G/C snv 0.28 0.30
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.080 0.875 8 2011 2019
dbSNP: rs873601
rs873601
0.677 0.360 13 102875987 3 prime UTR variant G/A snv 0.59
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2016 2016
dbSNP: rs26802
rs26802
0.925 0.160 3 10290681 intron variant T/G snv 0.31
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2014 2014
dbSNP: rs7911488
rs7911488
0.882 0.080 10 103394332 5 prime UTR variant A/G snv 0.34 0.26
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2015 2015
dbSNP: rs1360602468
rs1360602468
0.925 0.080 14 103698904 missense variant G/C;T snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2015 2015
dbSNP: rs745564626
rs745564626
0.752 0.280 14 103699003 missense variant C/G;T snv 4.3E-05
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2013 2013
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: rs1866074
rs1866074
TDG
1.000 0.080 12 103980664 non coding transcript exon variant A/G snv 0.40
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2019 2019
dbSNP: rs156697
rs156697
0.672 0.560 10 104279427 missense variant A/G;T snv 0.35
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2011 2011
dbSNP: rs11694911
rs11694911
1.000 0.080 2 10433072 regulatory region variant C/T snv 0.12
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2018 2018
dbSNP: rs2302615
rs2302615
0.807 0.120 2 10448012 intron variant C/T snv 0.31
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.020 1.000 2 2009 2018