List of variants in gene TNNI3 reported as likely benign for Hypertrophic cardiomyopathy 7

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_000363.5(TNNI3):c.244C>T (p.Pro82Ser)	rs77615401	0.00699
NM_000363.5(TNNI3):c.273G>A (p.Ala91=)	rs75491697	0.00188
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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