Source: CURATED

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: rs6983267
rs6983267
0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.900 0.945 15 2007 2019
dbSNP: rs267608140
rs267608140
0.925 0.160 2 47806838 missense variant T/A;C snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.700 1.000 12 1999 2012
dbSNP: rs63750157
rs63750157
1.000 0.080 2 47804943 missense variant T/C snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.700 1.000 12 1999 2012
dbSNP: rs63750358
rs63750358
1.000 0.080 2 47800037 missense variant G/C snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.700 1.000 12 1999 2012
dbSNP: rs63750637
rs63750637
1.000 0.080 2 47800343 missense variant C/G;T snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.700 1.000 12 1999 2012
dbSNP: rs137853148
rs137853148
1.000 0.080 8 17589479 missense variant C/T snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.800 1.000 11 1995 2015
dbSNP: rs267607894
rs267607894
0.925 0.160 3 37050628 missense variant T/A;C snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.700 1.000 11 1996 2008
dbSNP: rs63750217
rs63750217
0.807 0.240 3 37048955 missense variant G/A;C snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.700 1.000 11 1996 2008
dbSNP: rs63750303
rs63750303
0.882 0.160 3 37014485 missense variant G/A;T snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.700 1.000 11 1996 2008
dbSNP: rs63750437
rs63750437
0.925 0.160 3 37000977 missense variant G/A;C snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.700 1.000 11 1996 2008
dbSNP: rs63750718
rs63750718
1.000 0.080 3 37047589 missense variant A/G snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.700 1.000 11 1996 2008
dbSNP: rs121913400
rs121913400
0.683 0.360 3 41224610 missense variant C/A;G;T snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.800 1.000 10 2006 2015
dbSNP: rs180177032
rs180177032
1.000 0.080 7 140781623 missense variant C/A snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.800 1.000 10 2006 2015
dbSNP: rs180177033
rs180177033
1.000 0.080 7 140781620 missense variant A/C snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.800 1.000 10 2006 2015
dbSNP: rs4939827
rs4939827
0.708 0.160 18 48927093 intron variant T/A;C snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.900 0.964 10 2007 2019
dbSNP: rs16892766
rs16892766
0.716 0.240 8 116618444 intergenic variant A/C snv 9.3E-02
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.900 1.000 9 2008 2019
dbSNP: rs3802842
rs3802842
0.695 0.280 11 111300984 intron variant C/A snv 0.71
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.900 1.000 9 2008 2019
dbSNP: rs10505477
rs10505477
0.658 0.400 8 127395198 intron variant A/G snv 0.40
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.890 0.938 7 2007 2019
dbSNP: rs7014346
rs7014346
0.732 0.240 8 127412547 intron variant A/G snv 0.63
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.830 0.889 6 2008 2019
dbSNP: rs704017
rs704017
0.776 0.080 10 79059375 intron variant A/G snv 0.55
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.810 1.000 6 2014 2019
dbSNP: rs11255841
rs11255841
0.776 0.080 10 8697617 intergenic variant T/A snv 0.25
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.810 1.000 5 2014 2019
dbSNP: rs4779584
rs4779584
0.732 0.160 15 32702555 intergenic variant T/C snv 0.67
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.870 1.000 5 2008 2016
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 5 2010 2019
dbSNP: rs7229639
rs7229639
0.763 0.080 18 48924606 intron variant A/G snv 0.87
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.820 1.000 5 2014 2019
dbSNP: rs10774214
rs10774214
0.790 0.080 12 4259186 intron variant T/C snv 0.54
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.810 1.000 4 2013 2019