Gene entry
PARK7
Parkinsonism associated deglycase
- Chromosome
- 1
- Cytoband
- 1p36.23
- Variants (rsID)
- 8
PARK7 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 1 (region 1p36.23). Its official name is “Parkinsonism associated deglycase”. The reference table lists 8 variants (rsID) for this gene.
Clinically classified variants
3 reference-table entries with clinical significance.
- rs71653619Benignsingle nucleotide variantAutosomal recessive early-onset Parkinson disease 7|Renal cysts and diabetes syndrome
- rs74315352Likely benignsingle nucleotide variantAutosomal recessive early-onset Parkinson disease 7
- rs74315354Othersingle nucleotide variantParkinson Disease 7, Autosomal Recessive Early-Onset
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.