List of variants in gene TNNT2 reported as likely pathogenic by Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease, Montreal Heart Institute

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_001276345.2(TNNT2):c.341C>T (p.Ala114Val)	rs727504245	0.00002
NM_001276345.2(TNNT2):c.490-1G>C	rs111344408	0.00001
NM_001276345.2(TNNT2):c.803A>T (p.Lys268Ile)	rs397516482	0.00001
NM_001276345.2(TNNT2):c.385G>C (p.Glu129Gln)	rs1571627006
NM_001276345.2(TNNT2):c.445C>T (p.Arg149Cys)	rs397516465
NM_001276345.2(TNNT2):c.451del (p.Arg151fs)	rs730881115
NM_001276345.2(TNNT2):c.548G>A (p.Arg183Gln)	rs397516471
NM_001276345.2(TNNT2):c.784G>A (p.Glu262Lys)	rs727504488

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