Gene: CNGA3 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1261
Gene Symbol: CNGA3
CNGA3 		0.110 GeneticVariation disease BEFREE Mutations in the CNGA3 gene have been associated with complete and incomplete forms of total colour blindness (achromatopsia), a disorder characterized by reduced visual acuity, lack of colour discrimination, photophobia and nystagmus. 18445228 2008
Entrez Id: 1261
Gene Symbol: CNGA3
CNGA3 		0.110 GeneticVariation disease CLINVAR
Entrez Id: 1261
Gene Symbol: CNGA3
CNGA3 		0.110 Biomarker disease HPO