List of variants in gene MYH7 reported as likely pathogenic by Klaassen Lab, Charite University Medicine Berlin

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_000257.4(MYH7):c.1048T>A (p.Tyr350Asn)	rs730880863
NM_000257.4(MYH7):c.1283C>A (p.Ala428Asp)	rs727503266
NM_000257.4(MYH7):c.644C>T (p.Thr215Ile)	rs1892948780
NM_000257.4(MYH7):c.847T>G (p.Tyr283Asp)	rs397515482

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