"Eurofins Ntd Llc (ga)"[submitter] AND "LOC130061940"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 227169	NM_001614.5(ACTG1):c.72C>T (p.Asp24=)	ACTG1, LOC130061940	Single nucleotide variant (synonymous variant +1 more)	Autosomal dominant nonsyndromic hearing loss 20 +3 more	GBenign/Likely benign
Select item 385516	NM_001614.5(ACTG1):c.39C>T (p.Gly13=)	ACTG1, LOC130061940	Single nucleotide variant (synonymous variant +1 more)	not specified +3 more	GBenign/Likely benign