"Genome-Nilou Lab"[submitter] AND "CRYM"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 44241	NM_001376256.1(CRYM):c.864C>G (p.Thr288=)	CRYM	Single nucleotide variant (synonymous variant)	Autosomal dominant nonsyndromic hearing loss 40 +2 more	GBenign
Select item 44237	NM_001376256.1(CRYM):c.325-12T>C	CRYM	Single nucleotide variant (intron variant)	Autosomal dominant nonsyndromic hearing loss 40 +2 more	GBenign