DHX29 — 167 ClinVar variants

All ClinVar germline DHX29 variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 161 flagged for review →

6 Likely benign · 161 Uncertain significance

Full DHX29 gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions

⚑ Evidence disagreements 161

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 101

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

Predictors split 60

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

All DHX29 variants

Likely benign 6

Uncertain significance 161