ClinVar Miner

List of variants reported as likely pathogenic for Hypertrophic cardiomyopathy 7 by Victorian Clinical Genetics Services, Murdoch Childrens Research Institute

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_000363.5(TNNI3):c.485G>A (p.Arg162Gln)	rs397516354	0.00001
NM_000363.5(TNNI3):c.592C>G (p.Leu198Val)	rs727504285	0.00001

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