Gene entry

TNNT3

troponin T3, fast skeletal type

Chromosome: 11
Cytoband: 11p15.5
Variants (rsID): 10

TNNT3 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 11 (region 11p15.5). Its official name is “troponin T3, fast skeletal type”. The reference table lists 10 variants (rsID) for this gene.

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Clinically classified variants

3 reference-table entries with clinical significance.

rs16927166Benignsingle nucleotide variantArthrogryposis multiplex congenita distal|Distal arthrogryposis type 2B1
rs144957238Conflicting interpretationssingle nucleotide variant
rs199474721Pathogenicsingle nucleotide variantArthyrgryposis, distal, type 2B|Arthrogryposis, distal, type 2B2

Other listed variants

rs909116
rs3781956
rs72846741
rs73413025
rs78662878
rs78952134
rs200287895

Public references

NCBI Gene
Ensembl
ClinVar

Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.