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Gene entry

PDSS1

decaprenyl diphosphate synthase subunit 1

Chromosome
10
Cytoband
10p12.1
Variants (rsID)
20

PDSS1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 10 (region 10p12.1). Its official name is “decaprenyl diphosphate synthase subunit 1”. The reference table lists 20 variants (rsID) for this gene.

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Clinically classified variants

6 reference-table entries with clinical significance.

  • rs77826284Benignsingle nucleotide variantDeafness-encephaloneuropathy-obesity-valvulopathy syndrome
  • rs116424900Conflicting interpretationssingle nucleotide variantDeafness-encephaloneuropathy-obesity-valvulopathy syndrome
  • rs537781419Conflicting interpretationssingle nucleotide variantCoenzyme Q10 deficiency
  • rs762902803Conflicting interpretationssingle nucleotide variantDeafness-encephaloneuropathy-obesity-valvulopathy syndrome
  • rs116148064Likely benignsingle nucleotide variant
  • rs142182789Uncertain significancesingle nucleotide variantDeafness-encephaloneuropathy-obesity-valvulopathy syndrome

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.