"Genome-Nilou Lab"[submitter] AND "MYL3"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 255638	NM_000258.3(MYL3):c.307+37A>C	MYL3	Single nucleotide variant (intron variant)	Hypertrophic cardiomyopathy 8 +2 more	GBenign
Select item 255637	NM_000258.3(MYL3):c.129+44G>T	MYL3	Single nucleotide variant (intron variant)	Hypertrophic cardiomyopathy 8 +2 more	GBenign