"OMIM"[submitter] AND "STRC"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 4345	NC_000015.10:g.(?_43599438)_(43608225_43613711)del	STRC	Deletion	Autosomal recessive nonsyndromic hearing loss 16	GPathogenic
Select item 4343	NM_153700.2(STRC):c.3156dup (p.Cys1053fs)	STRC (C1053fs)	Duplication (frameshift variant)	Autosomal recessive nonsyndromic hearing loss 16	GPathogenic
Select item 4344	NM_153700.2(STRC):c.2171_2174del (p.Val724fs)	STRC (V724fs)	Deletion (frameshift variant)	Autosomal recessive nonsyndromic hearing loss 16	GPathogenic

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