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Gene entry

STAMBP

STAM binding protein

Chromosome
2
Cytoband
2p13.1
Variants (rsID)
12

STAMBP is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 2 (region 2p13.1). Its official name is “STAM binding protein”. The reference table lists 12 variants (rsID) for this gene.

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Clinically classified variants

4 reference-table entries with clinical significance.

  • rs77000353Benignsingle nucleotide variantMicrocephaly-capillary malformation syndrome
  • rs143739249Pathogenicsingle nucleotide variantMicrocephaly-capillary malformation syndrome
  • rs397509390Pathogenicsingle nucleotide variantMicrocephaly-capillary malformation syndrome
  • rs181632285Uncertain significancesingle nucleotide variant

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.