CLEC4F — 92 ClinVar variants

All ClinVar germline CLEC4F variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 80 flagged for review →

1 Conflicting · 2 Benign · 1 Benign/Likely benign · 12 Likely benign · 76 Uncertain significance

Full CLEC4F gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions

⚑ Evidence disagreements 80

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 52

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

Predictors split 27

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

All CLEC4F variants

Conflicting classifications of pathogenicity 1

Benign 2

Benign/Likely benign 1

Likely benign 12

Uncertain significance 76