Gene entry
RDH8
retinol dehydrogenase 8
- Chromosome
- 19
- Cytoband
- 19p13.2
- Variants (rsID)
- 5
RDH8 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 19 (region 19p13.2). Its official name is “retinol dehydrogenase 8”. The reference table lists 5 variants (rsID) for this gene.
Clinically classified variants
2 reference-table entries with clinical significance.
- rs1644731Not classifiedmissense_variantMyopia|Hypertension, Essential
- rs77833898Not classifiedmissense_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.