MYB — 84 ClinVar variants

All ClinVar germline MYB variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 43 flagged for review →

11 Benign · 1 Benign/Likely benign · 10 Likely benign · 62 Uncertain significance

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

⚑ Evidence disagreements 43

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 36

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

All MYB variants

Benign 11

Benign/Likely benign 1

Likely benign 10

Uncertain significance 62