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: rs353163
rs353163
0.882 0.080 4 67919056 missense variant T/A;C;G snv 0.67
Squamous cell carcinoma of esophagus
Digestive System Diseases; Neoplasms 0.040 1.000 4 2006 2013
dbSNP: rs353163
rs353163
0.882 0.080 4 67919056 missense variant T/A;C;G snv 0.67
CUI: C0546837
Disease: Malignant neoplasm of esophagus
Malignant neoplasm of esophagus
Digestive System Diseases; Neoplasms 0.020 1.000 2 2006 2013
dbSNP: rs353163
rs353163
0.882 0.080 4 67919056 missense variant T/A;C;G snv 0.67
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms
Digestive System Diseases; Neoplasms 0.020 1.000 2 2006 2013
dbSNP: rs353163
rs353163
0.882 0.080 4 67919056 missense variant T/A;C;G snv 0.67
CUI: C0152018
Disease: Esophageal carcinoma
Esophageal carcinoma
Digestive System Diseases; Neoplasms 0.020 1.000 2 2006 2013