CST2 — 48 ClinVar variants

All ClinVar germline CST2 variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 44 flagged for review →

1 Benign · 6 Likely benign · 41 Uncertain significance

Full CST2 gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions

⚑ Evidence disagreements 44

Variants where the independent computational evidence doesn't line up with the clinical picture — a QC signal for a second look, not a reclassification.

Predictors split 33

The independent predictors disagree with each other — read with care.

All CST2 variants

Benign 1

Likely benign 6

Uncertain significance 41