CXCL2 — 19 ClinVar variants

All ClinVar germline CXCL2 variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 15 flagged for review →

4 Likely benign · 15 Uncertain significance

Full CXCL2 gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions

⚑ Evidence disagreements 15

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 CXCL2 variants

Likely benign 4

Uncertain significance 15