List of variants in gene MYH11 reported as likely benign by Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease, Montreal Heart Institute

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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: 7

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HGVS	dbSNP	gnomAD frequency
NM_002474.3(MYH11):c.3816G>A (p.Glu1272=)	rs112990531	0.00038
NM_002474.3(MYH11):c.2893G>T (p.Ala965Ser)	rs113696032	0.00031
NM_002474.3(MYH11):c.342A>T (p.Ile114=)	rs746783926	0.00003
NM_002474.3(MYH11):c.2112G>A (p.Val704=)	rs781085663	0.00002
NM_002474.3(MYH11):c.1827C>T (p.Ala609=)	rs1177383353	0.00001
NM_002474.3(MYH11):c.3375G>C (p.Glu1125Asp)	rs779019646	0.00001
NM_002474.3(MYH11):c.1575+8del	rs769321167

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