ARID5A — 99 ClinVar variants

All ClinVar germline ARID5A variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 90 flagged for review →

1 Conflicting · 6 Likely benign · 92 Uncertain significance

Full ARID5A gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions

⚑ Evidence disagreements 90

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 87

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

Predictors split 2

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

All ARID5A variants

Conflicting classifications of pathogenicity 1

Likely benign 6

  • p.Ser455Gly Single submitter
  • c.571-4C>A No assertion criteria ARID5A-related disorder
  • p.Gly194Glu No assertion criteria ARID5A-related disorder
  • p.Leu304Pro No assertion criteria ARID5A-related disorder
  • p.Pro508= No assertion criteria ARID5A-related disorder
  • p.Val484= No assertion criteria ARID5A-related disorder

Uncertain significance 92