List of variants in gene TNNI3 reported as likely pathogenic by Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease, Montreal Heart Institute

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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: 6

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HGVS	dbSNP	gnomAD frequency
NM_000363.5(TNNI3):c.557G>A (p.Arg186Gln)	rs397516357	0.00001
NM_000363.5(TNNI3):c.592C>G (p.Leu198Val)	rs727504285	0.00001
NM_000363.5(TNNI3):c.204del (p.Arg69fs)	rs727504872
NM_000363.5(TNNI3):c.414G>C (p.Lys138Asn)
NM_000363.5(TNNI3):c.438A>T (p.Arg146Ser)	rs2085712265
NM_000363.5(TNNI3):c.529AAG[1] (p.Lys178del)	rs397516351

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