CCNG2 — 31 ClinVar variants

All ClinVar germline CCNG2 variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 26 flagged for review →

4 Benign · 1 Likely benign · 26 Uncertain significance

Full CCNG2 gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions

⚑ Evidence disagreements 26

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 CCNG2 variants

Benign 4

Likely benign 1

Uncertain significance 26