List of variants in gene MYBPC3 reported as likely pathogenic by Victorian Clinical Genetics Services, Murdoch Childrens Research Institute

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: 12

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HGVS	dbSNP	gnomAD frequency
NM_000256.3(MYBPC3):c.1591G>C (p.Gly531Arg)	rs397515912	0.00006
NM_000256.3(MYBPC3):c.1224-80G>A	rs1025692267	0.00005
NM_000256.3(MYBPC3):c.2429G>A (p.Arg810His)	rs375675796	0.00005
NC_000011.10:g.47332705G>C	rs730880592
NC_000011.10:g.47347065C>T	rs864622197
NM_000256.3(MYBPC3):c.1224-33G>A
NM_000256.3(MYBPC3):c.1591G>A (p.Gly531Arg)	rs397515912
NM_000256.3(MYBPC3):c.1645C>T (p.Gln549Ter)	rs2142860329
NM_000256.3(MYBPC3):c.1927+337G>T
NM_000256.3(MYBPC3):c.2362dup (p.Cys788fs)
NM_000256.3(MYBPC3):c.3599T>C (p.Leu1200Pro)	rs397516028
NM_000256.3(MYBPC3):c.852-2A>G	rs1565629792

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