"Genome-Nilou Lab"[submitter] AND "MYO6"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1181071	NM_004999.4(MYO6):c.817-21G>A	MYO6	Single nucleotide variant (intron variant)	Autosomal dominant nonsyndromic hearing loss 22 +2 more	GBenign
Select item 45147	NM_004999.4(MYO6):c.2658+17C>T	MYO6	Single nucleotide variant (intron variant)	Autosomal dominant nonsyndromic hearing loss 22 +3 more	GBenign
Select item 45130	NM_004999.4(MYO6):c.*12C>T	MYO6	Single nucleotide variant (3 prime UTR variant +1 more)	not specified +3 more	GBenign

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