ENO2 — 43 ClinVar variants

All ClinVar germline ENO2 variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 39 flagged for review →

1 Benign · 2 Likely benign · 40 Uncertain significance

Full ENO2 gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions

⚑ Evidence disagreements 39

Variants where the independent computational evidence doesn't line up with the clinical picture — a QC signal for a second look, not a reclassification.

All ENO2 variants

Benign 1

Likely benign 2

  • p.Asp142= No assertion criteria ENO2-related disorder
  • p.Leu137= No assertion criteria ENO2-related disorder

Uncertain significance 40