ANP32B — 27 ClinVar variants

All ClinVar germline ANP32B variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 21 flagged for review →

3 Benign · 2 Likely benign · 22 Uncertain significance

Full ANP32B 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 ANP32B variants

Benign 3

Likely benign 2

Uncertain significance 22