Gene entry
GP9
glycoprotein IX platelet
- Chromosome
- 3
- Cytoband
- 3q21.3
- Variants (rsID)
- 5
GP9 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 3 (region 3q21.3). Its official name is “glycoprotein IX platelet”. The reference table lists 5 variants (rsID) for this gene.
Clinically classified variants
4 reference-table entries with clinical significance.
- rs121918037Pathogenicsingle nucleotide variantBernard-Soulier syndrome type C|Macrothrombocytopenia|Bernard Soulier syndrome
- rs28933377Pathogenicsingle nucleotide variantBernard-Soulier syndrome type C
- rs28933378Pathogenicsingle nucleotide variantBernard-Soulier syndrome type C|Bernard Soulier syndrome
- rs5030764Pathogenicsingle nucleotide variantBernard-Soulier syndrome type C|Bernard Soulier syndrome|Macrothrombocytopenia|Thrombocytopenia
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.