List of variants in gene MYH7 reported as benign for Left ventricular noncompaction cardiomyopathy

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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.2967T>C (p.Ile989=)	rs7157716	0.43030
NM_000257.4(MYH7):c.732C>T (p.Phe244=)	rs2069542	0.27385
NM_000257.4(MYH7):c.1128C>T (p.Asp376=)	rs2231126	0.15761
NM_000257.4(MYH7):c.1062C>T (p.Gly354=)	rs735712	0.06133
NM_000257.4(MYH7):c.1605A>G (p.Glu535=)	rs2069543	0.03319

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