CGB2 — 36 ClinVar variants

All ClinVar germline CGB2 variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 30 flagged for review →

1 Benign · 6 Likely benign · 29 Uncertain significance

Full CGB2 gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions

⚑ Evidence disagreements 30

Variants where the independent computational evidence doesn't line up with the clinical picture — a QC signal for a second look, not a reclassification.

All CGB2 variants

Benign 1

Likely benign 6

Uncertain significance 29