CSNK2A2 — 42 ClinVar variants

All ClinVar germline CSNK2A2 variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 23 flagged for review →

18 Benign · 24 Uncertain significance

Full CSNK2A2 gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions

⚑ Evidence disagreements 23

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 CSNK2A2 variants

Benign 18

Uncertain significance 24