C1384666[trait identifier] AND "The Raphael Recanati Genetics Institut - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 996370	Single allele	GJB6	Deletion	Hearing impairment	GBenign
Select item 996368	Single allele	CATSPER2, CKMT1A +2 more	Deletion	Hearing impairment	GBenign
Select item 996369	Single allele	OTOA	Deletion	Hearing impairment	GBenign
Select item 617628	NM_133261.3(GIPC3):c.937T>C (p.Ter313Gln)	GIPC3	Single nucleotide variant (stop lost)	Hearing impairment	GUncertain significance

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