CCNYL1 — 36 ClinVar variants

All ClinVar germline CCNYL1 variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 32 flagged for review →

4 Likely benign · 32 Uncertain significance

Full CCNYL1 gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions

⚑ Evidence disagreements 32

Variants where the independent computational evidence doesn't line up with the clinical picture — a QC signal for a second look, not a reclassification.

All CCNYL1 variants

Likely benign 4

Uncertain significance 32