Gene: NR2E3 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 10002
Gene Symbol: NR2E3
NR2E3 		0.110 GeneticVariation phenotype BEFREE To determine the progression of cone vision loss in patients with recessive disease from NR2E3 gene mutations. 29971438 2018
Entrez Id: 10002
Gene Symbol: NR2E3
NR2E3 		0.110 Biomarker phenotype HPO