DMWD — 108 ClinVar variants

All ClinVar germline DMWD variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 97 flagged for review →

11 Benign · 1 Likely benign · 96 Uncertain significance

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

⚑ Evidence disagreements 97

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 50

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

Predictors split 47

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

All DMWD variants

Benign 11

  • p.Ala109= No assertion criteria DMWD-related disorder
  • p.Ala472= No assertion criteria DMWD-related disorder
  • p.Ala582Val No assertion criteria DMWD-related disorder ⚠
  • p.Gly120= No assertion criteria DMWD-related disorder
  • p.Gly415= No assertion criteria DMWD-related disorder
  • p.Pro294= No assertion criteria DMWD-related disorder
  • p.Pro417= No assertion criteria DMWD-related disorder
  • p.Pro454= No assertion criteria DMWD-related disorder
  • p.Pro471Ser No assertion criteria DMWD-related disorder
  • p.Ser559= No assertion criteria DMWD-related disorder
  • p.Thr527= No assertion criteria DMWD-related disorder

Likely benign 1

Uncertain significance 96