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: 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: 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: 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: rs1801133
rs1801133
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.100 0.818 11 2006 2019
dbSNP: rs6687758
rs6687758
0.763 0.200 1 221991606 regulatory region variant A/G snv 0.20
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.840 1.000 8 2010 2019
dbSNP: rs1051740
rs1051740
0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.070 0.714 7 2005 2013
dbSNP: rs1801131
rs1801131
0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.060 0.833 6 2008 2019
dbSNP: rs2234922
rs2234922
0.630 0.440 1 225838705 missense variant A/G;T snv 0.19; 2.8E-05
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.060 0.667 6 2005 2013
dbSNP: rs3219489
rs3219489
0.672 0.360 1 45331833 missense variant C/A;G snv 0.29 0.27
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.060 0.833 6 2008 2018
dbSNP: rs587780078
rs587780078
0.882 0.120 1 45331514 frameshift variant -/CC delins 1.6E-04 2.7E-04
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.700 1.000 6 2004 2012
dbSNP: rs587783057
rs587783057
0.925 0.120 1 45331676 stop gained G/A snv 1.2E-05
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.700 1.000 6 2005 2009
dbSNP: rs1805087
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.050 0.600 5 1999 2013
dbSNP: rs1342387
rs1342387
0.776 0.120 1 202945228 intron variant T/C snv 0.53
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.040 1.000 4 2011 2015
dbSNP: rs1800872
rs1800872
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.040 1.000 4 2012 2014
dbSNP: rs1800896
rs1800896
0.507 0.800 1 206773552 intron variant T/C snv 0.41
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.040 0.750 4 2009 2014
dbSNP: rs3024505
rs3024505
0.790 0.320 1 206766559 upstream gene variant G/A snv 0.11
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.040 1.000 4 2012 2015
dbSNP: rs529008617
rs529008617
0.851 0.160 1 45331529 missense variant G/A snv 7.2E-05 2.8E-05
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.700 1.000 4 2005 2010
dbSNP: rs587778536
rs587778536
0.882 0.120 1 45331700 frameshift variant G/- delins 6.4E-05 4.2E-05
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.700 1.000 4 2006 2009
dbSNP: rs587780088
rs587780088
0.882 0.120 1 45334493 stop gained G/A;C snv 8.0E-06; 4.0E-06
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.700 1.000 4 2008 2009
dbSNP: rs587782885
rs587782885
0.925 0.120 1 45332440 stop gained G/A;C snv 4.0E-06
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.700 1.000 4 2005 2009
dbSNP: rs1136410
rs1136410
0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.030 0.667 3 2010 2014
dbSNP: rs12733285
rs12733285
0.776 0.120 1 202952912 intron variant C/T snv 0.26
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.030 0.667 3 2011 2015
dbSNP: rs145204276
rs145204276
0.658 0.320 1 173868254 splice donor variant CAAGG/- delins 8.8E-02
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.030 1.000 3 2016 2018
dbSNP: rs587781628
rs587781628
0.882 0.120 1 45331558 splice acceptor variant T/C snv 2.4E-05 7.0E-06
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.700 1.000 3 2004 2005