Gene entry
SH3PXD2B
SH3 and PX domains 2B
- Chromosome
- 5
- Cytoband
- 5q35.1
- Variants (rsID)
- 27
SH3PXD2B is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 5 (region 5q35.1). Its official name is “SH3 and PX domains 2B”. The reference table lists 27 variants (rsID) for this gene.
Clinically classified variants
4 reference-table entries with clinical significance.
- rs2569232Benignsingle nucleotide variantFrank-Ter Haar syndrome
- rs869366Benignsingle nucleotide variantFrank-Ter Haar syndrome
- rs149519060Conflicting interpretationssingle nucleotide variant
- rs200536170Uncertain 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.