ClinVar Miner

List of variants reported as benign for Primary familial hypertrophic cardiomyopathy by Biesecker Lab/Clinical Genomics Section, National Institutes of Health

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Total variants: 4
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HGVS dbSNP gnomAD frequency
NM_001276345.2(TNNT2):c.788A>G (p.Lys263Arg) rs3730238 0.05965
NM_000256.3(MYBPC3):c.2686G>A (p.Val896Met) rs35078470 0.00601
NM_000256.3(MYBPC3):c.2992C>G (p.Gln998Glu) rs11570112 0.00247
NM_000257.4(MYH7):c.77C>T (p.Ala26Val) rs186964570 0.00021

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