FYN — 30 ClinVar variants

All ClinVar germline FYN variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 17 flagged for review →

3 Pathogenic · 6 Benign · 3 Likely benign · 18 Uncertain significance

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

⚑ Evidence disagreements 17

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.

All FYN variants

Pathogenic 3

  • p.Arg96Gly No assertion criteria EBV-positive nodal T- and NK-cell lymphoma
  • p.Arg96Trp No assertion criteria EBV-positive nodal T- and NK-cell lymphoma
  • p.Thr97Ala No assertion criteria EBV-positive nodal T- and NK-cell lymphoma ⚠

Benign 6

Likely benign 3

Uncertain significance 18