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 		0.130 GeneticVariation disease BEFREE So far, CNGA3 mutations are not only one of the most common causes of achromatopsia and cone dystrophy or cone-rod dystrophy but also one of the most commonly mutated genes among various forms of retinopathy. 30711023 2019
Entrez Id: 1261
Gene Symbol: CNGA3
CNGA3 		0.130 GeneticVariation disease BEFREE Homozygous missense variant in the human CNGA3 channel causes cone-rod dystrophy. 25052312 2015
Entrez Id: 1261
Gene Symbol: CNGA3
CNGA3 		0.130 GeneticVariation disease BEFREE Our results suggest that CNGA3 mutations are a common cause of cone-rod dystrophies and achromatopsia in the Chinese population. 24903488 2014
Entrez Id: 1261
Gene Symbol: CNGA3
CNGA3 		0.130 CausalMutation disease CLINVAR