UGT1A9 — 47 ClinVar variants

All ClinVar germline UGT1A9 variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 32 flagged for review →

2 Benign · 1 Benign/Likely benign · 8 Likely benign · 36 Uncertain significance

Full UGT1A9 gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions

⚑ Evidence disagreements 32

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 25

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

All UGT1A9 variants

Benign 2

Benign/Likely benign 1

Likely benign 8

  • p.Ala100Thr Single submitter
  • p.Tyr481= Single submitter
  • p.Ala144= No assertion criteria UGT1A9-related disorder
  • p.Cys3Tyr No assertion criteria UGT1A9-related disorder
  • p.Glu139= No assertion criteria UGT1A9-related disorder
  • p.Ser141= No assertion criteria UGT1A9-related disorder
  • p.Ser306= No assertion criteria UGT1A9-related disorder
  • p.Val167Ala No assertion criteria UGT1A9-related disorder

Uncertain significance 36