List of variants in gene MYBPC3 reported as likely pathogenic by Neuberg Centre For Genomic Medicine, NCGM

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_000256.3(MYBPC3):c.851+2T>C	rs1194615408	0.00001
NM_000256.3(MYBPC3):c.1483C>T (p.Arg495Trp)	rs397515905
NM_000256.3(MYBPC3):c.3020G>A (p.Trp1007Ter)	rs1565623533
NM_000256.3(MYBPC3):c.3158_3159del (p.Glu1053fs)

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