CCND3 — 31 ClinVar variants

All ClinVar germline CCND3 variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 28 flagged for review →

3 Benign · 28 Uncertain significance

Full CCND3 gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions

⚑ Evidence disagreements 28

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 CCND3 variants

Benign 3

Uncertain significance 28