DOP1B — 432 ClinVar variants

All ClinVar germline DOP1B variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 363 flagged for review →

1 Conflicting · 11 Benign · 1 Benign/Likely benign · 30 Likely benign · 389 Uncertain significance

Full DOP1B gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions

⚑ Evidence disagreements 363

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 296

ClinVar classifies these uncertain (VUS), but the independent predictors unanimously lean one way — a triage signal for review, not a reclassification. · showing the 150 best-reviewed of 296

Predictors split 66

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

All DOP1B variants

Conflicting classifications of pathogenicity 1

Benign 11

Benign/Likely benign 1

Likely benign 30

Uncertain significance 389

Showing the top 300 by review status; the full set is in the sitemap.