"Ambry Genetics"[submitter] AND "LOC111982869"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2070558	NM_022124.6(CDH23):c.7972A>C (p.Asn2658His)	CDH23, LOC111982869 (N2658H +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 1343702	NM_022124.6(CDH23):c.8057T>C (p.Val2686Ala)	CDH23, LOC111982869 (V2686A +1 more)	Single nucleotide variant (missense variant)	not specified +2 more	GUncertain significance