ARL4D — 27 ClinVar variants

All ClinVar germline ARL4D variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 21 flagged for review →

2 Likely benign · 25 Uncertain significance

Full ARL4D gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions

⚑ Evidence disagreements 21

Variants where the independent computational evidence doesn't line up with the clinical picture — a QC signal for a second look, not a reclassification.

All ARL4D variants

Likely benign 2

  • p.Ser13Ala Single submitter
  • p.His117Arg No assertion criteria EBV-positive nodal T- and NK-cell lymphoma

Uncertain significance 25