ARHGAP24 — 315 ClinVar variants

All ClinVar germline ARHGAP24 variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 169 flagged for review →

19 Conflicting · 56 Benign · 3 Benign/Likely benign · 82 Likely benign · 155 Uncertain significance

Full ARHGAP24 gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions

⚑ Evidence disagreements 169

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 92

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

Predictors split 63

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

All ARHGAP24 variants

Conflicting classifications of pathogenicity 19

Benign 56

Benign/Likely benign 3

Likely benign 82

Uncertain significance 155