MYO7B — 425 ClinVar variants

All ClinVar germline MYO7B variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 333 flagged for review →

43 Benign · 51 Likely benign · 331 Uncertain significance

Full MYO7B gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions

⚑ Evidence disagreements 333

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 250

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 250

Predictors split 83

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

All MYO7B variants

Benign 43

Likely benign 51

Uncertain significance 331

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