ARHGAP1 — 56 ClinVar variants

All ClinVar germline ARHGAP1 variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 49 flagged for review →

1 Conflicting · 3 Benign · 5 Likely benign · 47 Uncertain significance

Full ARHGAP1 gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions

⚑ Evidence disagreements 49

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 agree, ClinVar conflicts 1

ClinVar submitters conflict, but the independent predictors unanimously agree — a QC review flag, not a reclassification.

Predictors lean, ClinVar uncertain 30

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

All ARHGAP1 variants

Conflicting classifications of pathogenicity 1

Benign 3

Likely benign 5

Uncertain significance 47