List of variants in gene MYBPC3 reported as uncertain significance by Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center

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: 25

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HGVS	dbSNP	gnomAD frequency
NM_000256.3(MYBPC3):c.3682C>T (p.Arg1228Cys)	rs201312636	0.00063
NM_000256.3(MYBPC3):c.1246G>A (p.Gly416Ser)	rs371513491	0.00046
NM_000256.3(MYBPC3):c.461T>C (p.Ile154Thr)	rs373946195	0.00019
NM_000256.3(MYBPC3):c.529C>T (p.Arg177Cys)	rs193922385	0.00010
NM_000256.3(MYBPC3):c.2761C>G (p.Gln921Glu)	rs367729718	0.00006
NM_000256.3(MYBPC3):c.2179G>A (p.Val727Met)	rs564378953	0.00004
NM_000256.3(MYBPC3):c.3800G>A (p.Arg1267His)	rs730880142	0.00004
NM_000256.3(MYBPC3):c.787G>A (p.Gly263Arg)	rs373730381	0.00004
NM_000256.3(MYBPC3):c.2198G>A (p.Arg733His)	rs534345197	0.00003
NM_000256.3(MYBPC3):c.2909G>A (p.Arg970Gln)	rs727504346	0.00003
NM_000256.3(MYBPC3):c.133G>A (p.Gly45Arg)	rs775837337	0.00002
NM_000256.3(MYBPC3):c.1915G>A (p.Val639Ile)	rs780907679	0.00002
NM_000256.3(MYBPC3):c.2500C>T (p.Arg834Trp)	rs752007810	0.00002
NM_000256.3(MYBPC3):c.3103G>A (p.Ala1035Thr)	rs552505566	0.00002
NM_000256.3(MYBPC3):c.713G>A (p.Arg238His)	rs727504396	0.00002
NM_000256.3(MYBPC3):c.818G>A (p.Arg273His)	rs376461745	0.00002
NM_000256.3(MYBPC3):c.1039G>A (p.Gly347Ser)	rs397515884	0.00001
NM_000256.3(MYBPC3):c.2815C>T (p.Arg939Trp)	rs534366414	0.00001
NM_000256.3(MYBPC3):c.3358C>T (p.Arg1120Cys)	rs368721523	0.00001
NM_000256.3(MYBPC3):c.3613C>T (p.Arg1205Trp)	rs727503171	0.00001
NM_000256.3(MYBPC3):c.149G>A (p.Ser50Asn)	rs2142869623
NM_000256.3(MYBPC3):c.1828G>A (p.Asp610Asn)	rs371564200
NM_000256.3(MYBPC3):c.2864C>A (p.Pro955His)	rs2095880941
NM_000256.3(MYBPC3):c.3017C>A (p.Thr1006Asn)	rs778132423
NM_000256.3(MYBPC3):c.821+5G>A	rs397516077

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