NCOR1 — 319 ClinVar variants

All ClinVar germline NCOR1 variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 235 flagged for review →

1 Likely pathogenic · 19 Benign · 4 Benign/Likely benign · 44 Likely benign · 251 Uncertain significance

Full NCOR1 gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions

⚑ Evidence disagreements 235

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 183

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 183

Predictors split 51

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

All NCOR1 variants

Likely pathogenic 1

Benign 19

Benign/Likely benign 4

Likely benign 44

Uncertain significance 251