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Gene entry

PLCE1

phospholipase C epsilon 1

Chromosome
10
Cytoband
10q23.33
Variants (rsID)
72

PLCE1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 10 (region 10q23.33). Its official name is “phospholipase C epsilon 1”. The reference table lists 72 variants (rsID) for this gene.

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Clinically classified variants

11 reference-table entries with clinical significance.

  • rs111929795Benignsingle nucleotide variantNephrotic syndrome, type 3
  • rs141639885Benignsingle nucleotide variantNephrotic syndrome, type 3
  • rs17417407Benignsingle nucleotide variantNephrotic syndrome, type 3
  • rs2274223Benignsingle nucleotide variantNephrotic syndrome, type 3
  • rs3765524Benignsingle nucleotide variantNephrotic syndrome, type 3
  • rs58539480Benignsingle nucleotide variantNephrotic syndrome, type 3
  • rs61749239Conflicting interpretationssingle nucleotide variantNephrotic syndrome, type 3
  • rs61751493Conflicting interpretationssingle nucleotide variantNephrotic syndrome, type 3
  • rs121912605Pathogenicsingle nucleotide variantNephrotic syndrome, type 3
  • rs180753337Uncertain significancesingle nucleotide variant
  • rs192219615Uncertain significancesingle nucleotide variantNephrotic syndrome, type 3

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.