Source: GWASCAT

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: rs143046984
rs143046984
0.790 0.080 14 70937529 intron variant -/A delins 4.2E-02
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.710 1.000 1 2016 2016
dbSNP: rs202110856
rs202110856
0.790 0.080 5 96794169 intron variant -/C delins 2.1E-05
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.700 1.000 1 2015 2015
dbSNP: rs377429877
rs377429877
0.776 0.080 13 33518027 intron variant -/TAA delins 6.0E-02
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.700 1.000 1 2019 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 6 2008 2019
dbSNP: rs10911251
rs10911251
0.790 0.080 1 183112059 intron variant A/C snv 0.37
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.800 1.000 2 2013 2019
dbSNP: rs16973225
rs16973225
0.790 0.080 15 81937658 intron variant A/C snv 7.4E-02
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.700 1.000 1 2015 2015
dbSNP: rs2184857
rs2184857
0.790 0.080 1 239918447 upstream gene variant A/C snv 0.45
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.700 1.000 1 2017 2017
dbSNP: rs6058093
rs6058093
0.776 0.080 20 34625392 intron variant A/C snv 0.55
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.700 1.000 1 2019 2019
dbSNP: rs6720296
rs6720296
0.790 0.080 2 45181130 intron variant A/C snv 0.52
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.700 1.000 1 2015 2015
dbSNP: rs73975588
rs73975588
NXN
0.790 0.080 17 913501 intron variant A/C snv 9.9E-02
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.700 1.000 1 2019 2019
dbSNP: rs9924886
rs9924886
0.776 0.080 16 68710036 intron variant A/C snv 0.25
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.700 1.000 1 2019 2019
dbSNP: rs11150038
rs11150038
0.790 0.080 16 78042662 intron variant A/C;G snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.700 1.000 1 2015 2015
dbSNP: rs17102823
rs17102823
0.776 0.080 14 34894698 intergenic variant A/C;G snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.700 1.000 1 2018 2018
dbSNP: rs35107139
rs35107139
0.776 0.080 14 53952388 intron variant A/C;G;T snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.700 1.000 2 2019 2019
dbSNP: rs4768903
rs4768903
0.790 0.080 12 50651666 intron variant A/C;G;T snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.700 1.000 1 2015 2015
dbSNP: rs2250430
rs2250430
0.776 0.080 12 6312008 intron variant A/C;T snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.700 1.000 1 2019 2019
dbSNP: rs4450168
rs4450168
0.790 0.080 11 10265208 intron variant A/C;T snv 0.12
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.700 1.000 1 2019 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: 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: 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 4 2007 2019
dbSNP: rs11190164
rs11190164
0.776 0.080 10 99591947 intergenic variant A/G snv 0.19
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.700 1.000 3 2015 2019
dbSNP: rs1800469
rs1800469
0.547 0.760 19 41354391 intron variant A/G snv 0.69
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.810 1.000 3 2014 2018
dbSNP: rs2735940
rs2735940
0.689 0.400 5 1296371 upstream gene variant A/G snv 0.49
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.700 1.000 3 2019 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 3 2008 2019