Gene: USH2A ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 7399
Gene Symbol: USH2A
USH2A 		0.110 GeneticVariation phenotype BEFREE Interestingly, these same USH2A variants are also identified in another family with vision loss where subsequent clinical follow-up confirmed pre-existing hearing loss since early childhood, eventually resulting in a reassigned diagnosis of Usher syndrome. 31046701 2019
Entrez Id: 7399
Gene Symbol: USH2A
USH2A 		0.110 CausalMutation phenotype CLINVAR
Entrez Id: 7399
Gene Symbol: USH2A
USH2A 		0.110 Biomarker phenotype HPO