List of variants in gene MYBPC3 reported as benign by Biesecker Lab/Clinical Genomics Section, National Institutes of Health

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_000256.3(MYBPC3):c.706A>G (p.Ser236Gly)	rs3729989	0.09621
NM_000256.3(MYBPC3):c.472G>A (p.Val158Met)	rs3729986	0.06899
NM_000256.3(MYBPC3):c.1144C>T (p.Arg382Trp)	rs11570076	0.01409
NM_000256.3(MYBPC3):c.2498C>T (p.Ala833Val)	rs3729952	0.00756
NM_000256.3(MYBPC3):c.2686G>A (p.Val896Met)	rs35078470	0.00601
NM_000256.3(MYBPC3):c.530G>A (p.Arg177His)	rs201012766	0.00405
NM_000256.3(MYBPC3):c.977G>A (p.Arg326Gln)	rs34580776	0.00376
NM_000256.3(MYBPC3):c.2992C>G (p.Gln998Glu)	rs11570112	0.00247
NM_000256.3(MYBPC3):c.3106C>T (p.Arg1036Cys)	rs61729664	0.00128
NM_000256.3(MYBPC3):c.478C>T (p.Arg160Trp)	rs193068692	0.00047

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