ARHGAP8 — 86 ClinVar variants

All ClinVar germline ARHGAP8 variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 76 flagged for review →

3 Benign · 12 Likely benign · 71 Uncertain significance

Full ARHGAP8 gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions

⚑ Evidence disagreements 76

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 26

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

Predictors split 50

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

All ARHGAP8 variants

Benign 3

Likely benign 12

Uncertain significance 71