Gene entry
TRIM32
tripartite motif containing 32
- Chromosome
- 9
- Cytoband
- 9q33.1
- Variants (rsID)
- 10
TRIM32 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 9 (region 9q33.1). Its official name is “tripartite motif containing 32”. The reference table lists 10 variants (rsID) for this gene.
Clinically classified variants
6 reference-table entries with clinical significance.
- rs141352486Conflicting interpretationssingle nucleotide variantBardet-Biedl syndrome
- rs3747834Conflicting interpretationssingle nucleotide variantSarcotubular myopathy|Bardet-Biedl syndrome|Bardet-Biedl syndrome 11
- rs3747835Conflicting interpretationssingle nucleotide variantBardet-Biedl syndrome 11|Bardet-Biedl syndrome|Sarcotubular myopathy
- rs555217187Conflicting interpretationssingle nucleotide variantBardet-Biedl syndrome
- rs111033571Pathogenicsingle nucleotide variantBardet-Biedl syndrome 11|Bardet-Biedl syndrome
- rs121434447Uncertain significancesingle nucleotide variantSarcotubular myopathy|Bardet-Biedl syndrome|Bardet-Biedl syndrome 11
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.