C4760579[trait identifier] AND "Baylor Genetics"[submitter] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1030371	NM_001304438.2(TMEM132E):c.1228A>G (p.Met410Val)	TMEM132E (M410V)	Single nucleotide variant (missense variant)	Hearing loss, autosomal recessive 99	GUncertain significance
Select item 1030372	NM_001304438.2(TMEM132E):c.2730C>G (p.Ile910Met)	TMEM132E (I910M)	Single nucleotide variant (missense variant)	Hearing loss, autosomal recessive 99	GUncertain significance