CDNF — 3 ClinVar variants
All ClinVar germline CDNF variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 1 flagged for review →
2 Benign · 1 Uncertain significance
Full CDNF gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions⚑ Evidence disagreements 1
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 split 1
The independent predictors disagree with each other — read with care.
All CDNF variants
Benign 2
- p.Ala135Ser Multiple submitters
- p.Tyr167= Multiple submitters
Uncertain significance 1
- p.Ser121Arg Single submitter ⚠