Gene: HARS1 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3035
Gene Symbol: HARS1
HARS1 		0.110 GeneticVariation disease BEFREE The USH3B mutation, which encodes a Y454S substitution in HARS, is inherited in an autosomal recessive fashion and associated with childhood deafness, blindness, and episodic hallucinations during acute illness. 28632987 2017
Entrez Id: 3035
Gene Symbol: HARS1
HARS1 		0.110 Biomarker disease HPO