SRPRB — 36 ClinVar variants

All ClinVar germline SRPRB variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 31 flagged for review →

1 Conflicting · 1 Benign · 34 Uncertain significance

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

⚑ Evidence disagreements 31

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 lean, ClinVar uncertain 24

ClinVar classifies these uncertain (VUS), but the independent predictors unanimously lean one way — a triage signal for review, not a reclassification.

All SRPRB variants

Conflicting classifications of pathogenicity 1

Benign 1

Uncertain significance 34