FCGR1A — 44 ClinVar variants

All ClinVar germline FCGR1A variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 33 flagged for review →

1 Benign · 8 Likely benign · 35 Uncertain significance

Full FCGR1A gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions

⚑ Evidence disagreements 33

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 26

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

All FCGR1A variants

Benign 1

Likely benign 8

Uncertain significance 35