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

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_002471.4(MYH6):c.3302T>C (p.Val1101Ala)	rs365990	0.44987
NM_002471.4(MYH6):c.5598A>G (p.Leu1866=)	rs17091278	0.08756
NM_002471.4(MYH6):c.4011G>A (p.Ser1337=)	rs451794	0.07834
NM_002471.4(MYH6):c.4527G>A (p.Glu1509=)	rs34855944	0.02632
NM_002471.4(MYH6):c.2685G>A (p.Ala895=)	rs752345245	0.00006
NM_002471.4(MYH6):c.2547G>A (p.Lys849=)	rs770629886	0.00001
NM_002471.4(MYH6):c.3876G>A (p.Gln1292=)	rs145290322	0.00001

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