Gene entry
SATB2
SATB homeobox 2
- Chromosome
- 2
- Cytoband
- 2q33.1
- Variants (rsID)
- 21
SATB2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 2 (region 2q33.1). Its official name is “SATB homeobox 2”. The reference table lists 21 variants (rsID) for this gene.
Clinically classified variants
1 reference-table entries with clinical significance.
- rs137853127Pathogenicsingle nucleotide variantChromosome 2q32-q33 deletion syndrome|Cleft palate|Intellectual disability
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.