ATG2B — 388 ClinVar variants

All ClinVar germline ATG2B variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 241 flagged for review →

1 Conflicting · 92 Benign · 2 Benign/Likely benign · 40 Likely benign · 253 Uncertain significance

Full ATG2B gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions

⚑ Evidence disagreements 241

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 agree, ClinVar conflicts 1

ClinVar submitters conflict, but the independent predictors unanimously agree — a QC review flag, not a reclassification.

Predictors lean, ClinVar uncertain 203

ClinVar classifies these uncertain (VUS), but the independent predictors unanimously lean one way — a triage signal for review, not a reclassification. · showing the 150 best-reviewed of 203

Predictors split 37

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

All ATG2B variants

Conflicting classifications of pathogenicity 1

Benign 92

Benign/Likely benign 2

Likely benign 40

Uncertain significance 253