B3GNT3 — 59 ClinVar variants

All ClinVar germline B3GNT3 variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 46 flagged for review →

2 Benign · 9 Likely benign · 48 Uncertain significance

Full B3GNT3 gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions

⚑ Evidence disagreements 46

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 41

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

All B3GNT3 variants

Benign 2

Likely benign 9

Uncertain significance 48