"Genome Diagnostics Laboratory, University Medical Center Utrecht"[sub - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 138400	NM_000258.3(MYL3):c.482-17C>T	MYL3	Single nucleotide variant (intron variant)	Hypertrophic cardiomyopathy 8 +2 more	GBenign/Likely benign
Select item 1175080	NM_000258.3(MYL3):c.482-18G>A	MYL3	Single nucleotide variant (intron variant)	not specified +1 more	GLikely benign
Select item 1284346	NM_000258.3(MYL3):c.421G>A (p.Asp141Asn)	MYL3 (D141N)	Single nucleotide variant (missense variant)	Hypertrophic cardiomyopathy +2 more	GUncertain significance
Select item 227621	NM_000258.3(MYL3):c.307+15C>T	MYL3	Single nucleotide variant (intron variant)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 181441	NM_000258.3(MYL3):c.220G>A (p.Gly74Arg)	MYL3 (G74R)	Single nucleotide variant (missense variant)	Cardiomyopathy +4 more	GConflicting classifications of pathogenicity
Select item 177931	NM_000258.3(MYL3):c.187C>T (p.Arg63Cys)	MYL3 (R63C)	Single nucleotide variant (missense variant)	Cardiomyopathy +3 more	GUncertain significance
Select item 43119	NM_000258.3(MYL3):c.130-14G>T	MYL3	Single nucleotide variant (intron variant)	Hypertrophic cardiomyopathy +4 more	GBenign/Likely benign

ClinVar