NCOA3 — 173 ClinVar variants

All ClinVar germline NCOA3 variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 151 flagged for review →

1 Pathogenic · 1 Benign · 12 Likely benign · 159 Uncertain significance

Full NCOA3 gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions

⚑ Evidence disagreements 151

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 vs ClinVar 1

ClinVar calls these pathogenic, but the computational predictors lean tolerated — the highest-value review flag.

Predictors lean, ClinVar uncertain 130

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

All NCOA3 variants

Pathogenic 1

  • p.Ser937Cys Single submitter Bilateral sensorineural hearing impairment ⚠

Benign 1

Likely benign 12

Uncertain significance 159