List of variants in gene MYH6 reported as pathogenic for Hypertrophic cardiomyopathy 14

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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: 4

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HGVS	dbSNP	gnomAD frequency
NM_002471.4(MYH6):c.3195G>C (p.Gln1065His)	rs267606904	0.00015
NM_002471.4(MYH6):c.2384G>A (p.Arg795Gln)	rs267606907	0.00004
NM_002471.4(MYH6):c.1410+1G>A	rs1566513862
NM_002471.4(MYH6):c.4034T>C (p.Leu1345Pro)

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