List of variants in gene MYH7 reported as pathogenic for Left ventricular noncompaction 5

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_000257.4(MYH7):c.5378T>C (p.Leu1793Pro)	rs121913654
NM_000257.4(MYH7):c.5754C>R (p.Asn1918Lys)	rs138110910
NM_000257.4(MYH7):c.728G>A (p.Arg243His)	rs267606910
NM_000257.4(MYH7):c.732+1G>A	rs730880850
NM_000257.4(MYH7):c.847T>G (p.Tyr283Asp)	rs397515482

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