CUL2 — 76 ClinVar variants

All ClinVar germline CUL2 variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 68 flagged for review →

1 Likely pathogenic · 4 Benign · 1 Likely benign · 70 Uncertain significance

Full CUL2 gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions

⚑ Evidence disagreements 68

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

Predictors lean, ClinVar uncertain 54

ClinVar classifies these uncertain (VUS), but the independent predictors unanimously lean one way — a triage signal for review, not a reclassification.

All CUL2 variants

Likely pathogenic 1

  • p.Ile731Thr No assertion criteria Moyamoya angiopathy

Benign 4

Likely benign 1

Uncertain significance 70