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: rs1050631
rs1050631 		0.882 0.080 18 36114157 synonymous variant G/A snv 0.33 0.30
CUI: C0007137
Disease: Squamous cell carcinoma
Squamous cell carcinoma 		Neoplasms 0.800 1.000 1 2013 2013
dbSNP: rs1050631
rs1050631 		0.882 0.080 18 36114157 synonymous variant G/A snv 0.33 0.30
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms 		Digestive System Diseases; Neoplasms 0.700 1.000 1 2013 2013
dbSNP: rs7242481
rs7242481 		0.925 0.080 18 36129254 5 prime UTR variant G/A snv 0.35
CUI: C0007137
Disease: Squamous cell carcinoma
Squamous cell carcinoma 		Neoplasms 0.700 1.000 1 2013 2013
dbSNP: rs1050631
rs1050631 		0.882 0.080 18 36114157 synonymous variant G/A snv 0.33 0.30
CUI: C0279626
Disease: Squamous cell carcinoma of esophagus
Squamous cell carcinoma of esophagus 		Digestive System Diseases; Neoplasms 0.020 1.000 2 2013 2019
dbSNP: rs1050631
rs1050631 		0.882 0.080 18 36114157 synonymous variant G/A snv 0.33 0.30
CUI: C0278701
Disease: Gastric Adenocarcinoma
Gastric Adenocarcinoma 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2019 2019
dbSNP: rs7242481
rs7242481 		0.925 0.080 18 36129254 5 prime UTR variant G/A snv 0.35
CUI: C0279626
Disease: Squamous cell carcinoma of esophagus
Squamous cell carcinoma of esophagus 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2013 2013