"King Laboratory, University of Washington"[submitter] AND "OTOGL"[gen - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2445649	NM_001378609.3(OTOGL):c.4600+1G>T	OTOGL	Single nucleotide variant (splice donor variant)	Autosomal recessive nonsyndromic hearing loss 84B	GLikely pathogenic
Select item 499791	NM_001378609.3(OTOGL):c.6019+5G>A	OTOGL	Single nucleotide variant (intron variant)	not provided +1 more	GConflicting classifications of pathogenicity