C3888123[trait identifier] AND "OMIM"[submitter] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 866	NR_029512.1(MIR96):n.14C>A	MIR96	Single nucleotide variant (non-coding transcript variant)	Autosomal dominant nonsyndromic hearing loss 50	GPathogenic
Select item 865	NR_029512.1(MIR96):n.13G>A	MIR96	Single nucleotide variant (non-coding transcript variant)	Autosomal dominant nonsyndromic hearing loss 50	GPathogenic