List of variants in gene MYBPC3 reported as likely pathogenic by Clinical Genomics Laboratory, Stanford Medicine

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
NC_000011.10:g.47332282_47332306del	rs36212066
NM_000256.3(MYBPC3):c.2578_2590dup (p.Phe864fs)	rs2142855105
NM_000256.3(MYBPC3):c.3707_3708delinsGA (p.Leu1236Ter)
NM_000256.3(MYBPC3):c.3815-1G>A	rs397516044

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