"Blueprint Genetics"[submitter] AND "TNNC1"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 180550	NM_003280.3(TNNC1):c.469A>T (p.Met157Leu)	TNNC1 (M157L)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1Z +1 more	GUncertain significance
Select item 470558	NM_003280.3(TNNC1):c.400G>A (p.Glu134Lys)	TNNC1 (E134K)	Single nucleotide variant (missense variant)	TNNC1-related disorder +4 more	GUncertain significance