List of variants in gene MYBPC3 reported as benign by Mendelics

Minimum submission review status:		Collection method:
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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.833G>A (p.Gly278Glu)	rs147315081	0.00427
NM_000256.3(MYBPC3):c.530G>A (p.Arg177His)	rs201012766	0.00405
NM_000256.3(MYBPC3):c.2992C>G (p.Gln998Glu)	rs11570112	0.00247
NM_000256.3(MYBPC3):c.1519G>A (p.Gly507Arg)	rs35736435	0.00177
NM_000256.3(MYBPC3):c.3106C>T (p.Arg1036Cys)	rs61729664	0.00128
NM_000256.3(MYBPC3):c.3413G>A (p.Arg1138His)	rs187705120	0.00106
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.1286C>T (p.Ala429Val)	rs370412052	0.00036
NM_000256.3(MYBPC3):c.3535G>A (p.Glu1179Lys)	rs199669878	0.00036
NM_000256.3(MYBPC3):c.1855G>A (p.Glu619Lys)	rs200352299	0.00035
NM_000256.3(MYBPC3):c.82G>A (p.Val28Met)	rs776834755	0.00004
NM_000256.3(MYBPC3):c.2003G>A (p.Arg668His)	rs727503191	0.00002

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