ARHGAP23 — 293 ClinVar variants

All ClinVar germline ARHGAP23 variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 288 flagged for review →

7 Likely benign · 286 Uncertain significance

Full ARHGAP23 gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions

⚑ Evidence disagreements 288

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 148

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

Predictors split 140

The independent predictors disagree with each other — read with care.

All ARHGAP23 variants

Likely benign 7

Uncertain significance 286