Source: ALL
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: rs1063169
rs1063169 		0.925 0.080 14 75280415 5 prime UTR variant G/T snv 0.12
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2019 2019
dbSNP: rs1063169
rs1063169 		0.925 0.080 14 75280415 5 prime UTR variant G/T snv 0.12
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
Malignant neoplasm of colon and/or rectum 		0.010 1.000 1 2019 2019
dbSNP: rs7101
rs7101 		0.925 0.080 14 75278923 5 prime UTR variant C/T snv 0.77
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2019 2019
dbSNP: rs7101
rs7101 		0.925 0.080 14 75278923 5 prime UTR variant C/T snv 0.77
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
Malignant neoplasm of colon and/or rectum 		0.010 1.000 1 2019 2019
dbSNP: rs750949764
rs750949764 		1.000 0.040 14 75280958 missense variant G/C snv 4.0E-06
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis 		Pathological Conditions, Signs and Symptoms; Neoplasms 0.010 1.000 1 2018 2018
dbSNP: rs750949764
rs750949764 		1.000 0.040 14 75280958 missense variant G/C snv 4.0E-06
CUI: C0206732
Disease: Epithelioid hemangioendothelioma
Epithelioid hemangioendothelioma 		Neoplasms 0.010 1.000 1 2018 2018