CEP295NL, CEP295 N-terminal like, 100653515

N. diseases: 6; N. variants: 11
Disease: Eosinophilic esophagitis ×
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: rs3744790
rs3744790 		1.000 0.120 17 78897053 intron variant C/T snv 0.14
CUI: C0341106
Disease: Eosinophilic esophagitis
Eosinophilic esophagitis 		Digestive System Diseases; Immune System Diseases; Hemic and Lymphatic Diseases 0.700 1.000 1 2014 2014