NME2 — 2 ClinVar variants
All ClinVar germline NME2 variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 1 flagged for review →
1 Likely benign · 1 Uncertain significance
Full NME2 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 lean, ClinVar uncertain 1
ClinVar classifies these uncertain (VUS), but the independent predictors unanimously lean one way — a triage signal for review, not a reclassification.
All NME2 variants
Likely benign 1
- p.Ser120= Multiple submitters
Uncertain significance 1
- p.Lys12Asn Single submitter ⚠