DENND4B — 206 ClinVar variants

All ClinVar germline DENND4B variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 175 flagged for review →

1 Likely pathogenic · 1 Conflicting · 6 Benign · 24 Likely benign · 174 Uncertain significance

Full DENND4B gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions

⚑ Evidence disagreements 175

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 97

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

Predictors split 78

The independent predictors disagree with each other — read with care.

All DENND4B variants

Likely pathogenic 1

Conflicting classifications of pathogenicity 1

Benign 6

  • c.-6G>C No assertion criteria DENND4B-related disorder
  • p.Ala281= No assertion criteria DENND4B-related disorder
  • p.Gln901= No assertion criteria DENND4B-related disorder
  • p.Gly36= No assertion criteria DENND4B-related disorder
  • p.Thr1437= No assertion criteria DENND4B-related disorder
  • p.Tyr701= No assertion criteria DENND4B-related disorder

Likely benign 24

Uncertain significance 174