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 group BEFREE Since mutations in the CNGA3 gene may cause a variety of retinal dystrophies (complete and incomplete achromatopsia and progressive cone dystrophy), GNAT2 mutations may also prove to be implicated in other forms of retinal dystrophy with cone dysfunction. 12205108 2002
Entrez Id: 1261
Gene Symbol: CNGA3
CNGA3 		0.110 GeneticVariation group CLINVAR