List of variants in gene MYBPC3 reported as benign by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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: 17

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HGVS	dbSNP	gnomAD frequency
NM_000256.3(MYBPC3):c.2686G>A (p.Val896Met)	rs35078470	0.00601
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.565G>A (p.Val189Ile)	rs11570052	0.00187
NM_000256.3(MYBPC3):c.3106C>T (p.Arg1036Cys)	rs61729664	0.00128
NM_000256.3(MYBPC3):c.1564G>A (p.Ala522Thr)	rs11570082	0.00120
NM_000256.3(MYBPC3):c.3392T>C (p.Ile1131Thr)	rs370890951	0.00076
NM_000256.3(MYBPC3):c.649A>G (p.Ser217Gly)	rs138753870	0.00076
NM_000256.3(MYBPC3):c.3682C>T (p.Arg1228Cys)	rs201312636	0.00063
NM_000256.3(MYBPC3):c.3102C>T (p.Ala1034=)	rs200663253	0.00058
NM_000256.3(MYBPC3):c.478C>T (p.Arg160Trp)	rs193068692	0.00047
NM_000256.3(MYBPC3):c.3699G>A (p.Gln1233=)	rs200162906	0.00043
NM_000256.3(MYBPC3):c.471C>T (p.Phe157=)	rs150291001	0.00034
NM_000256.3(MYBPC3):c.2614G>A (p.Glu872Lys)	rs190765116	0.00012
NM_000256.3(MYBPC3):c.1457+20_1457+21delinsTT	rs2095890222
NM_000256.3(MYBPC3):c.3628-41_3628-17del	rs36212066
NM_000256.3(MYBPC3):c.705_706inv (p.Ser236Gly)

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