CGB7 — 43 ClinVar variants

All ClinVar germline CGB7 variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 39 flagged for review →

6 Likely benign · 37 Uncertain significance

Full CGB7 gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions

⚑ Evidence disagreements 39

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 CGB7 variants

Likely benign 6

Uncertain significance 37