C3AR1 — 78 ClinVar variants

All ClinVar germline C3AR1 variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 69 flagged for review →

1 Likely pathogenic · 2 Benign · 6 Likely benign · 69 Uncertain significance

Full C3AR1 gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions

⚑ Evidence disagreements 69

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 38

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

Predictors split 31

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

All C3AR1 variants

Likely pathogenic 1

  • p.Asp119fs No assertion criteria hemolytic uremic syndrome, atypical, susceptibility to, 1

Benign 2

Likely benign 6

Uncertain significance 69