DENND2B — 199 ClinVar variants

All ClinVar germline DENND2B variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 167 flagged for review →

9 Benign · 1 Benign/Likely benign · 9 Likely benign · 180 Uncertain significance

Full DENND2B gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions

⚑ Evidence disagreements 167

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 139

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

Predictors split 28

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

All DENND2B variants

Benign 9

Benign/Likely benign 1

Likely benign 9

Uncertain significance 180