ARHGAP22 — 148 ClinVar variants

All ClinVar germline ARHGAP22 variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 132 flagged for review →

2 Benign · 11 Likely benign · 135 Uncertain significance

Full ARHGAP22 gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions

⚑ Evidence disagreements 132

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 113

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

All ARHGAP22 variants

Benign 2

Likely benign 11

Uncertain significance 135