ARHGAP26 — 84 ClinVar variants

All ClinVar germline ARHGAP26 variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 67 flagged for review →

8 Benign · 10 Likely benign · 66 Uncertain significance

Full ARHGAP26 gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions

⚑ Evidence disagreements 67

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 44

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

All ARHGAP26 variants

Benign 8

Likely benign 10

Uncertain significance 66