ClinVar Miner

List of variants reported as likely pathogenic for Familial hypertrophic cardiomyopathy 4; Left ventricular noncompaction 10

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Total variants: 2
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HGVS dbSNP
NM_000256.3(MYBPC3):c.2148+1G>T rs1060499604
NM_000256.3(MYBPC3):c.2311G>A (p.Val771Met) rs371488302

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