ANKRD24 — 232 ClinVar variants

All ClinVar germline ANKRD24 variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 215 flagged for review →

1 Likely pathogenic · 14 Likely benign · 217 Uncertain significance

Full ANKRD24 gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions

⚑ Evidence disagreements 215

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 176

ClinVar classifies these uncertain (VUS), but the independent predictors unanimously lean one way — a triage signal for review, not a reclassification. · showing the 150 best-reviewed of 176

Predictors split 39

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

All ANKRD24 variants

Likely pathogenic 1

  • p.Thr645fs Single submitter Genetic hearing loss

Likely benign 14

Uncertain significance 217