DYNLL2 — 5 ClinVar variants
All ClinVar germline DYNLL2 variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 5 flagged for review →
5 Uncertain significance
Full DYNLL2 gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions⚑ Evidence disagreements 5
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 2
ClinVar classifies these uncertain (VUS), but the independent predictors unanimously lean one way — a triage signal for review, not a reclassification.
Predictors split 3
The independent predictors disagree with each other — read with care.
All DYNLL2 variants
Uncertain significance 5
- p.Glu45Asp Single submitter ⚠
- p.Ile34Met Single submitter ⚠
- p.Lys43Arg Single submitter ⚠
- p.Val22Ile Single submitter ⚠
- p.Val7Ala Single submitter ⚠