ADAMTSL3 — 350 ClinVar variants

All ClinVar germline ADAMTSL3 variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 244 flagged for review →

1 Conflicting · 89 Benign · 19 Likely benign · 241 Uncertain significance

Full ADAMTSL3 gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions

⚑ Evidence disagreements 244

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 agree, ClinVar conflicts 1

ClinVar submitters conflict, but the independent predictors unanimously agree — a QC review flag, not a reclassification.

Predictors lean, ClinVar uncertain 146

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

Predictors split 97

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

All ADAMTSL3 variants

Conflicting classifications of pathogenicity 1

Benign 89

Likely benign 19

Uncertain significance 241