List of variants in gene MYBPC3 reported as uncertain significance by Genetics and Genomics Program, Sidra 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: 6

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HGVS	dbSNP	gnomAD frequency
NM_000256.3(MYBPC3):c.3535G>A (p.Glu1179Lys)	rs199669878	0.00036
NM_000256.3(MYBPC3):c.814C>T (p.Arg272Cys)	rs397516075	0.00007
NM_000256.3(MYBPC3):c.2308G>A (p.Asp770Asn)	rs36211723	0.00002
NM_000256.3(MYBPC3):c.2504G>T (p.Arg835Leu)	rs527305885	0.00002
NM_000256.3(MYBPC3):c.495G>C (p.Glu165Asp)	rs730880619	0.00001
NM_000256.3(MYBPC3):c.654G>A (p.Lys218=)	rs2095898361

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