"NIHR Bioresource Rare Diseases, University of Cambridge"[submitter] A - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 438248	Single allele	LOC105378311, MIR548F1 +1 more	Deletion	Usher syndrome	GLikely pathogenic
Select item 438249	NM_001384140.1(PCDH15):c.475-2204_594+1766del	PCDH15	Deletion (splice acceptor variant +1 more)	Usher syndrome	GLikely pathogenic