RAD1 — 50 ClinVar variants

All ClinVar germline RAD1 variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 38 flagged for review →

4 Benign · 6 Likely benign · 40 Uncertain significance

Full RAD1 gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions

⚑ Evidence disagreements 38

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 28

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

All RAD1 variants

Benign 4

  • c.666-9C>G No assertion criteria RAD1-related disorder
  • p.Glu281Gly No assertion criteria RAD1-related disorder
  • p.Gly114Asp No assertion criteria RAD1-related disorder
  • p.Thr104Ser No assertion criteria RAD1-related disorder

Likely benign 6

  • p.Asp261= Single submitter
  • c.199-4A>G No assertion criteria RAD1-related disorder
  • c.666-10del No assertion criteria RAD1-related disorder
  • p.Leu93= No assertion criteria RAD1-related disorder
  • p.Thr173= No assertion criteria RAD1-related disorder
  • p.Tyr203Cys No assertion criteria RAD1-related disorder

Uncertain significance 40