ROR1 — 267 ClinVar variants

All ClinVar germline ROR1 variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 165 flagged for review →

1 Conflicting · 21 Benign · 6 Benign/Likely benign · 57 Likely benign · 182 Uncertain significance

Full ROR1 gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions

⚑ Evidence disagreements 165

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 136

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

Predictors split 29

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

All ROR1 variants

Conflicting classifications of pathogenicity 1

  • p.Glu452Asp Single submitter hearing loss, autosomal recessive 108 ⚠

Benign 21

Benign/Likely benign 6

Likely benign 57

Uncertain significance 182