CDC37 — 43 ClinVar variants

All ClinVar germline CDC37 variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 41 flagged for review →

3 Benign · 40 Uncertain significance

Full CDC37 gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions

⚑ Evidence disagreements 41

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 CDC37 variants

Benign 3

Uncertain significance 40