ARHGEF25 — 83 ClinVar variants

All ClinVar germline ARHGEF25 variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 62 flagged for review →

1 Likely pathogenic · 1 Benign · 1 Likely benign · 80 Uncertain significance

Full ARHGEF25 gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions

⚑ Evidence disagreements 62

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 vs ClinVar 1

ClinVar calls these pathogenic, but the computational predictors lean tolerated — the highest-value review flag.

Predictors lean, ClinVar uncertain 50

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

All ARHGEF25 variants

Likely pathogenic 1

Benign 1

Likely benign 1

Uncertain significance 80