SNRPB2 — 20 ClinVar variants

All ClinVar germline SNRPB2 variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 18 flagged for review →

1 Likely benign · 19 Uncertain significance

Full SNRPB2 gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions

⚑ Evidence disagreements 18

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 SNRPB2 variants

Likely benign 1

Uncertain significance 19