NT5M — 37 ClinVar variants

All ClinVar germline NT5M variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 34 flagged for review →

2 Likely benign · 35 Uncertain significance

Full NT5M gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions

⚑ Evidence disagreements 34

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 NT5M variants

Likely benign 2

Uncertain significance 35