Gene entry
SRCAP
Snf2 related CREBBP activator protein
- Chromosome
- 16
- Cytoband
- 16p11.2
- Variants (rsID)
- 7
SRCAP is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 16 (region 16p11.2). Its official name is “Snf2 related CREBBP activator protein”. The reference table lists 7 variants (rsID) for this gene.
Clinically classified variants
5 reference-table entries with clinical significance.
- rs117804715Benignsingle nucleotide variant
- rs189892751Benignsingle nucleotide variant
- rs199469464Pathogenicsingle nucleotide variantFloating-Harbor syndrome|Inborn genetic diseases|See cases|Neurodevelopmental delay
- rs199469465Pathogenicsingle nucleotide variantFloating-Harbor syndrome|Inborn genetic diseases
- rs201658767Uncertain 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.