List of variants in gene TNNT2 reported as uncertain significance for Left ventricular noncompaction cardiomyopathy

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: 11

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HGVS	dbSNP	gnomAD frequency
NM_001276345.2(TNNT2):c.692T>C (p.Ile231Thr)	rs45520032	0.00015
NM_001276345.2(TNNT2):c.52+7G>A	rs374443596	0.00007
NM_001276345.2(TNNT2):c.601-8C>T	rs397516475	0.00006
NM_001276345.2(TNNT2):c.720-5T>G	rs730881092	0.00004
NM_001276345.2(TNNT2):c.691A>G (p.Ile231Val)	rs886045828	0.00003
NM_001276345.2(TNNT2):c.233+6T>C	rs397516449	0.00001
NM_001276345.2(TNNT2):c.-1C>A	rs776936911
NM_001276345.2(TNNT2):c.-22G>C	rs886045829
NM_001276345.2(TNNT2):c.-22G>T	rs886045829
NM_001276345.2(TNNT2):c.270C>G (p.Pro90=)	rs140245123
NM_001276345.2(TNNT2):c.665T>A (p.Leu222Gln)	rs750800588

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