Disease: Esophageal Atresia ×
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: rs104893648
rs104893648 		0.882 0.320 2 15945883 missense variant G/A;T snv
CUI: C0014850
Disease: Esophageal Atresia
Esophageal Atresia 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases 0.700 0
dbSNP: rs779000620
rs779000620 		1.000 0.080 2 15942288 missense variant C/G snv 4.2E-06 7.0E-06
CUI: C0014850
Disease: Esophageal Atresia
Esophageal Atresia 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases 0.010 1.000 1 2006 2006