Gene: CEP290 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 80184
Gene Symbol: CEP290
CEP290 		0.110 GeneticVariation disease BEFREE Species-dependent splice recognition of a cryptic exon resulting from a recurrent intronic CEP290 mutation that causes congenital blindness. 25761237 2015
Entrez Id: 80184
Gene Symbol: CEP290
CEP290 		0.110 Biomarker disease HPO
Entrez Id: 80184
Gene Symbol: CEP290
CEP290 		0.110 CausalMutation disease CLINVAR