UTRN — 597 ClinVar variants

All ClinVar germline UTRN variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 340 flagged for review →

1 Likely pathogenic · 4 Conflicting · 79 Benign · 3 Benign/Likely benign · 40 Likely benign · 470 Uncertain significance

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

⚑ Evidence disagreements 340

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 agree, ClinVar conflicts 3

ClinVar submitters conflict, but the independent predictors unanimously agree — a QC review flag, not a reclassification.

Predictors lean, ClinVar uncertain 311

ClinVar classifies these uncertain (VUS), but the independent predictors unanimously lean one way — a triage signal for review, not a reclassification. · showing the 150 best-reviewed of 311

Predictors split 26

The independent predictors disagree with each other — read with care.

All UTRN variants

Likely pathogenic 1

  • c.4134+1G>A Single submitter Duchenne muscular dystrophy

Conflicting classifications of pathogenicity 4

Benign 79

Benign/Likely benign 3

Likely benign 40

Uncertain significance 470

Showing the top 300 by review status; the full set is in the sitemap.