UGT1A7 — 58 ClinVar variants

All ClinVar germline UGT1A7 variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 37 flagged for review →

1 Conflicting · 1 Benign · 11 Likely benign · 45 Uncertain significance

Full UGT1A7 gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions

⚑ Evidence disagreements 37

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 1

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

Predictors lean, ClinVar uncertain 23

ClinVar classifies these uncertain (VUS), but the independent predictors unanimously lean one way — a triage signal for review, not a reclassification.

All UGT1A7 variants

Conflicting classifications of pathogenicity 1

Benign 1

Likely benign 11

Uncertain significance 45