Gene entry
TNNT1
troponin T1, slow skeletal type
- Chromosome
- 19
- Cytoband
- 19q13.42
- Variants (rsID)
- 9
TNNT1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 19 (region 19q13.42). Its official name is “troponin T1, slow skeletal type”. The reference table lists 9 variants (rsID) for this gene.
Clinically classified variants
3 reference-table entries with clinical significance.
- rs28362592Benignsingle nucleotide variant
- rs3760873Benignsingle nucleotide variant
- rs138664823Conflicting interpretationssingle nucleotide variantNemaline myopathy 5
Other listed variants
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.