List of variants in gene MYH6 reported as likely benign by Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease, Montreal Heart Institute

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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: 9

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HGVS	dbSNP	gnomAD frequency
NM_002471.4(MYH6):c.3883G>C (p.Glu1295Gln)	rs34935550	0.00217
NM_002471.4(MYH6):c.1763A>C (p.Asp588Ala)	rs142992009	0.00153
NM_002471.4(MYH6):c.4136C>T (p.Thr1379Met)	rs145611185	0.00036
NM_002471.4(MYH6):c.5476G>A (p.Gly1826Ser)	rs202141059	0.00013
NM_002471.4(MYH6):c.4047C>T (p.Tyr1349=)	rs570555040	0.00006
NM_002471.4(MYH6):c.2364G>A (p.Thr788=)	rs779838927	0.00003
NM_002471.4(MYH6):c.1131C>T (p.Asp377=)	rs61742472
NM_002471.4(MYH6):c.5477G>A (p.Gly1826Asp)	rs200260229
NM_002471.4(MYH6):c.678C>G (p.Pro226=)	rs768893926

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