List of variants reported as likely pathogenic for Hypertrophic cardiomyopathy 7

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Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_000363.5(TNNI3):c.484C>T (p.Arg162Trp)	rs368861241	0.00004
NM_000363.5(TNNI3):c.421C>T (p.Arg141Trp)	rs730881071	0.00001
NM_000363.5(TNNI3):c.485G>A (p.Arg162Gln)	rs397516354	0.00001
NM_000363.5(TNNI3):c.497C>T (p.Ser166Phe)	rs727504242	0.00001
NM_000363.5(TNNI3):c.557G>A (p.Arg186Gln)	rs397516357	0.00001
NM_000363.5(TNNI3):c.586G>A (p.Asp196Asn)	rs104894727	0.00001
NM_000363.5(TNNI3):c.592C>G (p.Leu198Val)	rs727504285	0.00001
NM_000363.5(TNNI3):c.407G>A (p.Arg136Gln)	rs730881069
NM_000363.5(TNNI3):c.455A>G (p.Asp152Gly)
NM_000363.5(TNNI3):c.574C>T (p.Arg192Cys)	rs727503499

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