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Gene entry

DIS3L2

DIS3 like 3'-5' exoribonuclease 2

Chromosome
2
Cytoband
2q37.1
Variants (rsID)
67

DIS3L2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 2 (region 2q37.1). Its official name is “DIS3 like 3'-5' exoribonuclease 2”. The reference table lists 67 variants (rsID) for this gene.

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Clinically classified variants

14 reference-table entries with clinical significance.

  • rs148474013Benignsingle nucleotide variantPerlman syndrome
  • rs184764939Benignsingle nucleotide variantPerlman syndrome
  • rs723044Benignsingle nucleotide variantPerlman syndrome
  • rs143680532Conflicting interpretationssingle nucleotide variantPerlman syndrome
  • rs186340144Conflicting interpretationssingle nucleotide variantPerlman syndrome
  • rs186865544Conflicting interpretationssingle nucleotide variantPerlman syndrome
  • rs202042951Conflicting interpretationssingle nucleotide variantPerlman syndrome
  • rs369113667Conflicting interpretationssingle nucleotide variantPerlman syndrome
  • rs376299829Conflicting interpretationssingle nucleotide variantPerlman syndrome
  • rs377644356Conflicting interpretationssingle nucleotide variantPerlman syndrome
  • rs539081624Conflicting interpretationssingle nucleotide variantPerlman syndrome
  • rs760229466Conflicting interpretationssingle nucleotide variantPerlman syndrome
  • rs183901077Uncertain significancesingle nucleotide variantPerlman syndrome
  • rs199879981Uncertain significancesingle nucleotide variantPerlman 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.