UGT1A8 — 68 ClinVar variants

All ClinVar germline UGT1A8 variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 38 flagged for review →

1 Conflicting · 18 Benign · 10 Likely benign · 39 Uncertain significance

Full UGT1A8 gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions

⚑ Evidence disagreements 38

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 30

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

All UGT1A8 variants

Conflicting classifications of pathogenicity 1

Benign 18

Likely benign 10

Uncertain significance 39