CSNK1G3 — 35 ClinVar variants

All ClinVar germline CSNK1G3 variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 31 flagged for review →

1 Benign · 3 Likely benign · 31 Uncertain significance

Full CSNK1G3 gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions

⚑ Evidence disagreements 31

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 CSNK1G3 variants

Benign 1

  • c.1186-6A>G No assertion criteria CSNK1G3-related disorder

Likely benign 3

  • c.1186-4A>G No assertion criteria CSNK1G3-related disorder
  • p.Ser393= No assertion criteria CSNK1G3-related disorder
  • p.Thr451= No assertion criteria CSNK1G3-related disorder

Uncertain significance 31