C2750472[trait identifier] AND "Illumina Laboratory Services, Illumina - ClinVar - NCBI

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 346128	NM_003280.3(TNNC1):c.*127C>T	TNNC1	Single nucleotide variant (3 prime UTR variant)	Dilated cardiomyopathy 1Z +2 more	GConflicting classifications of pathogenicity
Select item 346129	NM_003280.3(TNNC1):c.*83A>C	TNNC1	Single nucleotide variant (3 prime UTR variant)	Dilated cardiomyopathy 1Z +2 more	GBenign/Likely benign
Select item 346130	NM_003280.3(TNNC1):c.*75G>A	TNNC1	Single nucleotide variant (3 prime UTR variant)	Dilated cardiomyopathy 1Z +1 more	GUncertain significance
Select item 700167	NM_003280.3(TNNC1):c.444C>T (p.Ile148=)	TNNC1	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +2 more	GConflicting classifications of pathogenicity
Select item 44679	NM_003280.3(TNNC1):c.387G>C (p.Thr129=)	TNNC1	Single nucleotide variant (synonymous variant)	not provided +4 more	GConflicting classifications of pathogenicity
Select item 702219	NM_003280.3(TNNC1):c.213G>C (p.Thr71=)	TNNC1	Single nucleotide variant (synonymous variant)	Hypertrophic cardiomyopathy 13 +2 more	GConflicting classifications of pathogenicity
Select item 44677	NM_003280.3(TNNC1):c.210C>T (p.Gly70=)	TNNC1	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +5 more	GConflicting classifications of pathogenicity
Select item 179034	NM_003280.3(TNNC1):c.108C>A (p.Ile36=)	TNNC1	Single nucleotide variant (synonymous variant)	not specified +5 more	GConflicting classifications of pathogenicity
Select item 346131	NM_003280.3(TNNC1):c.81C>T (p.Phe27=)	TNNC1	Single nucleotide variant (synonymous variant)	Dilated cardiomyopathy 1Z +2 more	GConflicting classifications of pathogenicity
Select item 346132	NM_003280.3(TNNC1):c.55+9C>A	TNNC1	Single nucleotide variant (intron variant)	Dilated cardiomyopathy 1Z +2 more	GConflicting classifications of pathogenicity
Select item 346133	NM_003280.3(TNNC1):c.4G>A (p.Asp2Asn)	TNNC1 (D2N)	Single nucleotide variant (missense variant)	Hypertrophic cardiomyopathy 13 +1 more	GUncertain significance