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Gene entry

STX11

syntaxin 11

Chromosome
6
Cytoband
6q24.2
Variants (rsID)
20

STX11 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 6 (region 6q24.2). Its official name is “syntaxin 11”. The reference table lists 20 variants (rsID) for this gene.

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Clinically classified variants

6 reference-table entries with clinical significance.

  • rs146949718Benignsingle nucleotide variantFamilial hemophagocytic lymphohistiocytosis 4|Autoinflammatory syndrome
  • rs3734228Benignsingle nucleotide variantFamilial hemophagocytic lymphohistiocytosis 4
  • rs45574234Benignsingle nucleotide variantFamilial hemophagocytic lymphohistiocytosis 4|Autoinflammatory syndrome
  • rs6912580Benignsingle nucleotide variantFamilial hemophagocytic lymphohistiocytosis 4
  • rs141499372Conflicting interpretationssingle nucleotide variantFamilial hemophagocytic lymphohistiocytosis 4|Autoinflammatory syndrome
  • rs145347140Uncertain significancesingle nucleotide variantFamilial hemophagocytic lymphohistiocytosis|Familial hemophagocytic lymphohistiocytosis 4

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.