C2673760[trait identifier] AND "OMIM"[submitter] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 17004	NM_004004.6(GJB2):c.35del (p.Gly12fs)	GJB2 (G12fs)	Deletion	Nonsyndromic genetic hearing loss	GPathogenic FDA Recognized database
Select item 5546	del(GJB6-D13S1830)	CRYL1, GJB2 +15 more	Deletion	Autosomal recessive nonsyndromic hearing loss 1A +2 more	GPathogenic
Select item 5548	NC_000013.11:g.(20228574_20228587)_(20460616_20460629)del	CRYL1, GJB6 +8 more	Deletion	Deafness, digenic, GJB2/GJB6	GPathogenic

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