"Hereditary Research Laboratory, Bethlehem University"[submitter] AND - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 402254	NM_001379180.1(ESRRB):c.608G>A (p.Arg203His)	ESRRB (R182H +1 more)	Single nucleotide variant (missense variant)	Autosomal recessive nonsyndromic hearing loss 35	GPathogenic
Select item 402255	NM_001379180.1(ESRRB):c.850G>A (p.Gly284Ser)	ESRRB (G263S +1 more)	Single nucleotide variant (missense variant)	Autosomal recessive nonsyndromic hearing loss 35	GPathogenic