Gene entry
PDYN
prodynorphin
- Chromosome
- 20
- Cytoband
- 20p13
- Variants (rsID)
- 17
PDYN 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 “prodynorphin”. The reference table lists 17 variants (rsID) for this gene.
Clinically classified variants
9 reference-table entries with clinical significance.
- rs149056587Benignsingle nucleotide variant
- rs185551108Benignsingle nucleotide variant
- rs1997794Benignsingle nucleotide variantAutosomal dominant cerebellar ataxia
- rs59191035Benignsingle nucleotide variant
- rs910079Benignsingle nucleotide variantSpinocerebellar ataxia type 23
- rs910080Benignsingle nucleotide variantSpinocerebellar ataxia type 23
- rs201486601Pathogenicsingle nucleotide variantSpinocerebellar ataxia type 23
- rs267606939Pathogenicsingle nucleotide variantSpinocerebellar ataxia type 23
- rs267606940Uncertain significancesingle nucleotide variantSpinocerebellar ataxia type 23
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.