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Gene entry

RDH5

retinol dehydrogenase 5

Chromosome
12
Cytoband
12q13.2
Variants (rsID)
3

RDH5 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 12 (region 12q13.2). Its official name is “retinol dehydrogenase 5”. The reference table lists 3 variants (rsID) for this gene.

Clinically classified variants

1 reference-table entries with clinical significance.

  • rs62638195Conflicting interpretationssingle nucleotide variantPigmentary retinal dystrophy

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.