PSMB11 — 69 ClinVar variants

All ClinVar germline PSMB11 variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 55 flagged for review →

4 Benign · 1 Benign/Likely benign · 5 Likely benign · 59 Uncertain significance

Full PSMB11 gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions

⚑ Evidence disagreements 55

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 45

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

All PSMB11 variants

Benign 4

Benign/Likely benign 1

Likely benign 5

Uncertain significance 59