List of variants in gene MYH6 reported as likely pathogenic for not provided

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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: 3

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HGVS	dbSNP	gnomAD frequency
NM_002471.4(MYH6):c.1108C>T (p.Arg370Trp)	rs753444140	0.00003
NM_002471.4(MYH6):c.4097C>T (p.Ala1366Val)	rs1085307922	0.00001
NM_002471.4(MYH6):c.1203C>A (p.Cys401Ter)	rs786205484

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