List of variants in gene MYBPC3 reported as uncertain significance 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: 6

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HGVS	dbSNP	gnomAD frequency
NM_000256.3(MYBPC3):c.2980C>T (p.Leu994Phe)	rs375776406	0.00019
NM_000256.3(MYBPC3):c.2176C>T (p.Arg726Cys)	rs752200396	0.00011
NC_000011.10:g.47342826T>C	rs886039119
NM_000256.3(MYBPC3):c.1227-7C>T
NM_000256.3(MYBPC3):c.292+1G>A	rs1433492944
NM_000256.3(MYBPC3):c.2994G>T (p.Gln998His)

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