List of variants reported as likely benign for Hypertrophic cardiomyopathy 7

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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_000363.5(TNNI3):c.244C>T (p.Pro82Ser)	rs77615401	0.00699
NM_001256715.2(DNAAF3):c.1248G>A (p.Val416=)	rs111250144	0.00398
NM_000363.5(TNNI3):c.273G>A (p.Ala91=)	rs75491697	0.00198
NM_000363.5(TNNI3):c.235C>T (p.Arg79Cys)	rs3729712	0.00048
NM_000363.5(TNNI3):c.*35C>T	rs375447438	0.00004
NM_000363.5(TNNI3):c.-98C>A	rs12973773

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