List of variants in gene MYH7 reported as uncertain significance for See cases

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: 11

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HGVS	dbSNP	gnomAD frequency
NM_000257.4(MYH7):c.3286G>T (p.Asp1096Tyr)	rs45478699	0.00013
NM_000257.4(MYH7):c.5471A>G (p.Asn1824Ser)	rs760218400	0.00003
NM_000257.4(MYH7):c.5470A>G (p.Asn1824Asp)	rs769112519	0.00002
NM_000257.4(MYH7):c.1456C>A (p.Gln486Lys)	rs1186558363
NM_000257.4(MYH7):c.2923-5G>A	rs779010466
NM_000257.4(MYH7):c.3007C>T (p.His1003Tyr)
NM_000257.4(MYH7):c.3086A>C (p.Gln1029Pro)	rs1892569039
NM_000257.4(MYH7):c.452C>T (p.Pro151Leu)	rs730880837
NM_000257.4(MYH7):c.5395G>A (p.Glu1799Lys)	rs730880816
NM_000257.4(MYH7):c.5659G>T (p.Glu1887Ter)	rs2138635468
NM_000257.4(MYH7):c.5751CAA[1] (p.Asn1918del)	rs1892067860

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