List of variants in gene MYBPC3 reported as 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: 5

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HGVS	dbSNP	gnomAD frequency
NM_000256.3(MYBPC3):c.1624+4A>T	rs397515916	0.00003
NC_000011.10:g.47337730dup	rs397515963	0.00002
NM_000256.3(MYBPC3):c.26-2A>G	rs376395543	0.00002
NM_000256.3(MYBPC3):c.3034C>T (p.Gln1012Ter)	rs730880586
NM_000256.3(MYBPC3):c.772+1G>A	rs397516072

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