CCDC91 — 56 ClinVar variants

All ClinVar germline CCDC91 variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 52 flagged for review →

2 Benign · 3 Likely benign · 51 Uncertain significance

Full CCDC91 gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions

⚑ Evidence disagreements 52

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 29

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

All CCDC91 variants

Benign 2

Likely benign 3

Uncertain significance 51