USP13 — 128 ClinVar variants

All ClinVar germline USP13 variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 115 flagged for review →

2 Benign · 1 Benign/Likely benign · 3 Likely benign · 122 Uncertain significance

Full USP13 gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions

⚑ Evidence disagreements 115

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 86

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

Predictors split 29

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

All USP13 variants

Benign 2

Benign/Likely benign 1

Likely benign 3

Uncertain significance 122