F2RL3 — 88 ClinVar variants

All ClinVar germline F2RL3 variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 70 flagged for review →

4 Benign · 8 Likely benign · 76 Uncertain significance

Full F2RL3 gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions

⚑ Evidence disagreements 70

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 61

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

All F2RL3 variants

Benign 4

Likely benign 8

Uncertain significance 76