ASB3 — 3 ClinVar variants
All ClinVar germline ASB3 variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 2 flagged for review →
1 Likely benign · 2 Uncertain significance
Full ASB3 gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions⚑ Evidence disagreements 2
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 2
ClinVar classifies these uncertain (VUS), but the independent predictors unanimously lean one way — a triage signal for review, not a reclassification.
All ASB3 variants
Likely benign 1
- p.Cys295= Single submitter
Uncertain significance 2
- p.Asp294Gly Single submitter ⚠
- p.Gln309Arg Single submitter ⚠