EIF3G — 34 ClinVar variants

All ClinVar germline EIF3G variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 30 flagged for review →

1 Benign · 2 Likely benign · 31 Uncertain significance

Full EIF3G gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions

⚑ Evidence disagreements 30

Variants where the independent computational evidence doesn't line up with the clinical picture — a QC signal for a second look, not a reclassification.

All EIF3G variants

Benign 1

Likely benign 2

Uncertain significance 31