List of variants reported as pathogenic for Hypertrophic cardiomyopathy 7 by OMIM

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Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_000363.5(TNNI3):c.586G>A (p.Asp196Asn)	rs104894727	0.00001
NM_000363.5(TNNI3):c.433C>G (p.Arg145Gly)	rs104894724
NM_000363.5(TNNI3):c.547_549del (p.Lys183del)	rs2147283135
NM_000363.5(TNNI3):c.569A>G (p.Asp190Gly)	rs104894728
NM_000363.5(TNNI3):c.607G>A (p.Gly203Ser)	rs267607127
NM_000363.5(TNNI3):c.616A>C (p.Lys206Gln)	rs104894725
NM_000363.5(TNNI3):c.61C>T (p.Arg21Cys)	rs267607128

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