"Genome-Nilou Lab"[submitter] AND "MYO9A"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1223022	NM_006901.4(MYO9A):c.3771A>G (p.Arg1257=)	MYO9A	Single nucleotide variant (synonymous variant)	Myasthenic syndrome, congenital, 24, presynaptic +1 more	GBenign
Select item 1225670	NM_006901.4(MYO9A):c.3578G>A (p.Gly1193Glu)	MYO9A (G1193E)	Single nucleotide variant (missense variant)	Myasthenic syndrome, congenital, 24, presynaptic +1 more	GBenign
Select item 1289337	NM_006901.4(MYO9A):c.1253+24A>G	MYO9A	Single nucleotide variant (intron variant)	not provided +1 more	GBenign

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