Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Gene entry

PRODH

proline dehydrogenase 1

Chromosome
22
Cytoband
22q11.21
Variants (rsID)
16

PRODH is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 22 (region 22q11.21). Its official name is “proline dehydrogenase 1”. The reference table lists 16 variants (rsID) for this gene.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Clinically classified variants

5 reference-table entries with clinical significance.

  • rs11913840Benignsingle nucleotide variantProline dehydrogenase deficiency|Schizophrenia 4|Proline dehydrogenase deficiency
  • rs2238731Benignsingle nucleotide variantProline dehydrogenase deficiency
  • rs450046Benignsingle nucleotide variantProline dehydrogenase deficiency|Schizophrenia 4
  • rs4819756Benignsingle nucleotide variantProline dehydrogenase deficiency
  • rs2904552Conflicting interpretationssingle nucleotide variantProline dehydrogenase deficiency|Schizophrenia 4

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.