DCAF4L2 — 73 ClinVar variants

All ClinVar germline DCAF4L2 variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 55 flagged for review →

3 Benign · 12 Likely benign · 58 Uncertain significance

Full DCAF4L2 gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions

⚑ Evidence disagreements 55

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 48

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

All DCAF4L2 variants

Benign 3

  • p.Arg47= No assertion criteria DCAF4L2-related disorder
  • p.Asn313Ser No assertion criteria DCAF4L2-related disorder
  • p.Phe146= No assertion criteria DCAF4L2-related disorder

Likely benign 12

Uncertain significance 58