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Gene entry

TNNI2

troponin I2, fast skeletal type

Chromosome
11
Cytoband
11p15.5
Variants (rsID)
8

TNNI2 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 I2, fast skeletal type”. The reference table lists 8 variants (rsID) for this gene.

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Clinically classified variants

7 reference-table entries with clinical significance.

  • rs907610Benignsingle nucleotide variantArthrogryposis multiplex congenita|Distal arthrogryposis type 2B1
  • rs139399106Conflicting interpretationssingle nucleotide variantArthrogryposis multiplex congenita distal|Arthrogryposis multiplex congenita
  • rs141400587Conflicting interpretationssingle nucleotide variant
  • rs181679318Conflicting interpretationssingle nucleotide variantArthrogryposis multiplex congenita|Arthrogryposis multiplex congenita distal
  • rs200110633Conflicting interpretationssingle nucleotide variantArthrogryposis multiplex congenita|Arthrogryposis multiplex congenita distal
  • rs104894311Pathogenicsingle nucleotide variantDistal arthrogryposis type 2B1
  • rs104894312Pathogenicsingle nucleotide variantDistal arthrogryposis type 2B1|Ulnar deviation of the wrist|Calcaneovalgus deformity|Distal arthrogryposis|Congenital finger flexion contractures

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.