List of variants in gene TNNC1 reported as uncertain significance for Primary dilated 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_003280.3(TNNC1):c.442A>G (p.Ile148Val)	rs397516848	0.00001
NM_003280.3(TNNC1):c.25G>A (p.Val9Ile)	rs1578264552
NM_003280.3(TNNC1):c.469A>T (p.Met157Leu)	rs730880230

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