Gene entry
CSNK2A1
casein kinase 2 alpha 1
- Chromosome
- 20
- Cytoband
- 20p13
- Variants (rsID)
- 14
CSNK2A1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 20 (region 20p13). Its official name is “casein kinase 2 alpha 1”. The reference table lists 14 variants (rsID) for this gene.
Clinically classified variants
5 reference-table entries with clinical significance.
- rs869312840Conflicting interpretationssingle nucleotide variantOkur-Chung neurodevelopmental syndrome|Inborn genetic diseases|See cases|Neurodevelopmental delay
- rs869312845Pathogenicsingle nucleotide variantOkur-Chung neurodevelopmental syndrome|Inborn genetic diseases
- rs869312846Pathogenicsingle nucleotide variantOkur-Chung neurodevelopmental syndrome
- rs869312848Pathogenicsingle nucleotide variantOkur-Chung neurodevelopmental syndrome
- rs869312849Pathogenicsingle nucleotide variantOkur-Chung neurodevelopmental syndrome
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.