ADGRB3 — 161 ClinVar variants

All ClinVar germline ADGRB3 variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 143 flagged for review →

2 Likely pathogenic · 2 Likely benign · 157 Uncertain significance

Full ADGRB3 gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions

⚑ Evidence disagreements 143

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 110

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

Predictors split 33

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

All ADGRB3 variants

Likely pathogenic 2

Likely benign 2

Uncertain significance 157