List of variants in gene MYBPC3 reported as uncertain significance for Primary dilated cardiomyopathy

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_000256.3(MYBPC3):c.3682C>T (p.Arg1228Cys)	rs201312636	0.00060
NM_000256.3(MYBPC3):c.3535G>A (p.Glu1179Lys)	rs199669878	0.00036
NM_000256.3(MYBPC3):c.1721G>A (p.Arg574Gln)	rs397515922	0.00026
NM_000256.3(MYBPC3):c.961G>A (p.Val321Met)	rs200119454	0.00024
NM_000256.3(MYBPC3):c.814C>T (p.Arg272Cys)	rs397516075	0.00007
NM_000256.3(MYBPC3):c.2311G>A (p.Val771Met)	rs371488302	0.00003
NM_000256.3(MYBPC3):c.1814A>G (p.Asp605Gly)	rs372371774	0.00002
NM_000256.3(MYBPC3):c.1091C>T (p.Ala364Val)	rs778161908	0.00001
NM_000256.3(MYBPC3):c.1433C>T (p.Ser478Leu)	rs730880540	0.00001
NM_000256.3(MYBPC3):c.1826C>T (p.Ala609Val)	rs730880553	0.00001
NM_000256.3(MYBPC3):c.742G>T (p.Asp248Tyr)	rs768625454	0.00001
NM_000256.3(MYBPC3):c.3812G>C (p.Arg1271Pro)	rs762225417
NM_000256.3(MYBPC3):c.93C>A (p.Ala31=)	rs397516085

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