Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs2585428
rs2585428
0.763 0.200 20 54170358 intron variant C/T snv 0.46
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
Digestive System Diseases; Neoplasms 0.020 0.500 2 2020 2020
dbSNP: rs4809960
rs4809960
0.807 0.240 20 54169534 intron variant T/C snv 0.20
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
Digestive System Diseases; Neoplasms 0.020 1.000 2 2020 2020
dbSNP: rs4809957
rs4809957
0.763 0.240 20 54154632 3 prime UTR variant A/G snv 0.29
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
Digestive System Diseases; Neoplasms 0.010 1.000 1 2017 2017
dbSNP: rs6022990
rs6022990
1.000 0.080 20 54158993 missense variant A/G snv 6.6E-03 2.8E-02
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
Digestive System Diseases; Neoplasms 0.010 1.000 1 2014 2014
dbSNP: rs6022999
rs6022999
0.790 0.160 20 54171474 intron variant A/G snv 0.36
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
Digestive System Diseases; Neoplasms 0.010 1.000 1 2020 2020
dbSNP: rs6068816
rs6068816
0.752 0.200 20 54164552 synonymous variant C/T snv 0.12 8.9E-02
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
Digestive System Diseases; Neoplasms 0.010 1.000 1 2020 2020