C2675236[trait identifier] AND "Laboratory of Prof. Karen Avraham, Tel - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 6491	NM_024009.3(GJB3):c.101T>C (p.Leu34Pro)	GJB3 (L34P)	Single nucleotide variant (missense variant)	Autosomal dominant nonsyndromic hearing loss 2B	GPathogenic
Select item 1402757	NM_024009.3(GJB3):c.302G>A (p.Arg101Gln)	GJB3 (R101Q)	Single nucleotide variant (missense variant)	Autosomal dominant nonsyndromic hearing loss 2B +1 more	GConflicting classifications of pathogenicity