CCL11 — 20 ClinVar variants

All ClinVar germline CCL11 variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 19 flagged for review →

2 Benign · 1 Likely benign · 17 Uncertain significance

Full CCL11 gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions

⚑ Evidence disagreements 19

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 CCL11 variants

Benign 2

Likely benign 1

  • p.Val28= No assertion criteria CCL11-related disorder

Uncertain significance 17