CST11 — 24 ClinVar variants

All ClinVar germline CST11 variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 21 flagged for review →

3 Likely benign · 21 Uncertain significance

Full CST11 gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions

⚑ Evidence disagreements 21

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 CST11 variants

Likely benign 3

Uncertain significance 21