List of variants in gene MYH7 reported as not provided for hypertrophic cardiomyopathy

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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: 7

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HGVS	dbSNP	gnomAD frequency
NM_000257.4(MYH7):c.2681A>G (p.Glu894Gly)	rs397516161	0.00001
NM_000257.4(MYH7):c.209C>T (p.Thr70Ile)	rs1327007939
NM_000257.4(MYH7):c.3711G>C (p.Gln1237His)	rs1361182615
NM_000257.4(MYH7):c.3727-15T>A
NM_000257.4(MYH7):c.3727-17T>A
NM_000257.4(MYH7):c.3727-21T>A
NM_000257.4(MYH7):c.4156C>T (p.Leu1386Phe)	rs727504703

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