List of variants in gene TNNT2 reported as pathogenic by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_001276345.2(TNNT2):c.310C>T (p.Arg104Cys)	rs727503513
NM_001276345.2(TNNT2):c.358T>A (p.Phe120Ile)	rs121964858
NM_001276345.2(TNNT2):c.451C>T (p.Arg151Trp)	rs74315379
NM_001276345.2(TNNT2):c.650AGA[3] (p.Lys220del)	rs45578238
NM_001276345.2(TNNT2):c.891G>A (p.Trp297Ter)	rs730881116

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