Gene entry
TNNC1
troponin C1, slow skeletal and cardiac type
- Chromosome
- 3
- Cytoband
- 3p21.1
- Variants (rsID)
- 7
TNNC1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 3 (region 3p21.1). Its official name is “troponin C1, slow skeletal and cardiac type”. The reference table lists 7 variants (rsID) for this gene.
Clinically classified variants
7 reference-table entries with clinical significance.
- rs141505676Conflicting interpretationssingle nucleotide variantHypertrophic cardiomyopathy 13|Dilated cardiomyopathy 1Z|Hypertrophic cardiomyopathy 13|Dilated cardiomyopathy 1Z|Cardiomyopathy
- rs202000367Conflicting interpretationssingle nucleotide variantHypertrophic cardiomyopathy 13|Dilated cardiomyopathy 1Z|Dilated cardiomyopathy 1Z|Hypertrophic cardiomyopathy 13|Cardiovascular phenotype|Cardiomyopathy
- rs397516845Conflicting interpretationssingle nucleotide variantDilated cardiomyopathy 1Z|Hypertrophic cardiomyopathy 13|Cardiovascular phenotype|Dilated cardiomyopathy 1Z|Hypertrophic cardiomyopathy 13
- rs267607125Likely pathogenicsingle nucleotide variantHypertrophic cardiomyopathy 13|Cardiovascular phenotype|Hypertrophic cardiomyopathy|Hypertrophic cardiomyopathy 13|Dilated cardiomyopathy 1Z|Cardiomyopathy
- rs876661393Likely pathogenicsingle nucleotide variant
- rs267607123Uncertain significancesingle nucleotide variantHypertrophic cardiomyopathy 13|Hypertrophic cardiomyopathy 13|Dilated cardiomyopathy 1Z
- rs267607124Uncertain significancesingle nucleotide variantHypertrophic cardiomyopathy 13|Hypertrophic cardiomyopathy 13|Dilated cardiomyopathy 1Z|Dilated cardiomyopathy 1S|Cardiovascular phenotype
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.