SYNRG — 156 ClinVar variants

All ClinVar germline SYNRG variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 129 flagged for review →

1 Benign · 20 Likely benign · 135 Uncertain significance

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

⚑ Evidence disagreements 129

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 107

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

All SYNRG variants

Benign 1

  • p.Pro962= No assertion criteria SYNRG-related disorder

Likely benign 20

Uncertain significance 135