Source: ALL

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: rs1017621656
rs1017621656
0.925 0.080 19 41352923 missense variant A/C;G snv 1.9E-05
CUI: C0699790
Disease: Colon Carcinoma
Colon Carcinoma
0.010 1.000 1 2001 2001
dbSNP: rs10222633
rs10222633
0.925 0.080 3 122258079 intron variant G/A snv 0.45
CUI: C0699790
Disease: Colon Carcinoma
Colon Carcinoma
0.010 1.000 1 2017 2017
dbSNP: rs1039659576
rs1039659576
MTR
0.689 0.520 1 236803473 missense variant A/G snv
CUI: C0699790
Disease: Colon Carcinoma
Colon Carcinoma
0.010 1.000 1 2005 2005
dbSNP: rs10411210
rs10411210
0.742 0.160 19 33041394 intron variant C/T snv 0.22
CUI: C0699790
Disease: Colon Carcinoma
Colon Carcinoma
0.010 1.000 1 2013 2013
dbSNP: rs1042522
rs1042522
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67
CUI: C0699790
Disease: Colon Carcinoma
Colon Carcinoma
0.010 1.000 1 2006 2006
dbSNP: rs1042636
rs1042636
0.672 0.360 3 122284922 missense variant A/G snv 0.15 9.0E-02
CUI: C0699790
Disease: Colon Carcinoma
Colon Carcinoma
0.010 1.000 1 2017 2017
dbSNP: rs1044129
rs1044129
0.790 0.200 15 33866065 3 prime UTR variant A/G;T snv
CUI: C0699790
Disease: Colon Carcinoma
Colon Carcinoma
0.010 1.000 1 2013 2013
dbSNP: rs10450310
rs10450310
0.925 0.080 10 52764898 downstream gene variant G/A snv 0.29
CUI: C0699790
Disease: Colon Carcinoma
Colon Carcinoma
0.010 1.000 1 2012 2012
dbSNP: rs1045485
rs1045485
0.637 0.480 2 201284866 missense variant G/A;C;T snv 4.0E-06; 9.0E-02
CUI: C0699790
Disease: Colon Carcinoma
Colon Carcinoma
0.010 1.000 1 2006 2006
dbSNP: rs1051753269
rs1051753269
0.790 0.120 7 55174029 missense variant G/A snv 7.0E-06
CUI: C0699790
Disease: Colon Carcinoma
Colon Carcinoma
0.010 1.000 1 2014 2014
dbSNP: rs1057519725
rs1057519725
0.851 0.320 12 25225627 missense variant G/A snv 7.0E-06
CUI: C0699790
Disease: Colon Carcinoma
Colon Carcinoma
0.010 1.000 1 2019 2019
dbSNP: rs1057519822
rs1057519822
0.925 0.080 15 66481818 missense variant T/A snv
CUI: C0699790
Disease: Colon Carcinoma
Colon Carcinoma
0.010 1.000 1 2019 2019
dbSNP: rs1060503118
rs1060503118
0.925 0.080 7 5987422 missense variant C/T snv
CUI: C0699790
Disease: Colon Carcinoma
Colon Carcinoma
0.010 1.000 1 2015 2015
dbSNP: rs10741657
rs10741657
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65
CUI: C0699790
Disease: Colon Carcinoma
Colon Carcinoma
0.010 1.000 1 2013 2013
dbSNP: rs10759932
rs10759932
0.732 0.560 9 117702866 upstream gene variant T/C snv 0.18
CUI: C0699790
Disease: Colon Carcinoma
Colon Carcinoma
0.010 < 0.001 1 2016 2016
dbSNP: rs10958713
rs10958713
0.925 0.080 8 42323198 intron variant C/T snv 0.28
CUI: C0699790
Disease: Colon Carcinoma
Colon Carcinoma
0.010 1.000 1 2013 2013
dbSNP: rs1130409
rs1130409
0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42
CUI: C0699790
Disease: Colon Carcinoma
Colon Carcinoma
0.010 1.000 1 2008 2008
dbSNP: rs1131691014
rs1131691014
0.439 0.800 17 7676154 frameshift variant -/C ins
CUI: C0699790
Disease: Colon Carcinoma
Colon Carcinoma
0.010 1.000 1 2006 2006
dbSNP: rs1131691029
rs1131691029
0.827 0.160 17 7673794 missense variant C/G snv
CUI: C0699790
Disease: Colon Carcinoma
Colon Carcinoma
0.010 1.000 1 2006 2006
dbSNP: rs1136410
rs1136410
0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15
CUI: C0699790
Disease: Colon Carcinoma
Colon Carcinoma
0.010 < 0.001 1 2009 2009
dbSNP: rs11536898
rs11536898
0.882 0.080 9 117717932 3 prime UTR variant C/A snv 0.14
CUI: C0699790
Disease: Colon Carcinoma
Colon Carcinoma
0.010 1.000 1 2012 2012
dbSNP: rs11539752
rs11539752
0.882 0.120 14 24632383 missense variant G/C snv 0.21 0.26
CUI: C0699790
Disease: Colon Carcinoma
Colon Carcinoma
0.010 < 0.001 1 2015 2015
dbSNP: rs11615
rs11615
0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55
CUI: C0699790
Disease: Colon Carcinoma
Colon Carcinoma
0.010 1.000 1 2019 2019
dbSNP: rs11625206
rs11625206
0.925 0.080 14 70727436 3 prime UTR variant C/T snv 0.26
CUI: C0699790
Disease: Colon Carcinoma
Colon Carcinoma
0.010 1.000 1 2012 2012
dbSNP: rs11721827
rs11721827
0.851 0.200 4 186069983 intron variant A/C snv 0.12
CUI: C0699790
Disease: Colon Carcinoma
Colon Carcinoma
0.010 1.000 1 2012 2012