List of variants reported as likely pathogenic for Hypertrophic cardiomyopathy 7 by 3billion

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_000363.5(TNNI3):c.421C>T (p.Arg141Trp)	rs730881071	0.00001
NM_000363.5(TNNI3):c.455A>G (p.Asp152Gly)	rs2085712121	0.00001
NM_000363.5(TNNI3):c.151-1G>A
NM_000363.5(TNNI3):c.485G>C (p.Arg162Pro)	rs397516354

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