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Gene entry

SH3BP2

SH3 domain binding protein 2

Chromosome
4
Cytoband
4p16.3
Variants (rsID)
17

SH3BP2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 4 (region 4p16.3). Its official name is “SH3 domain binding protein 2”. The reference table lists 17 variants (rsID) for this gene.

Clinically classified variants

4 reference-table entries with clinical significance.

  • rs190648042Benignsingle nucleotide variantFibrous dysplasia of jaw
  • rs231399Benignsingle nucleotide variantFibrous dysplasia of jaw
  • rs73189445Benignsingle nucleotide variantFibrous dysplasia of jaw
  • rs121909146Pathogenicsingle nucleotide variantFibrous dysplasia of jaw

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.