RAET1L — 54 ClinVar variants

All ClinVar germline RAET1L variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 45 flagged for review →

2 Benign · 8 Likely benign · 44 Uncertain significance

Full RAET1L gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions

⚑ Evidence disagreements 45

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 35

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

All RAET1L variants

Benign 2

Likely benign 8

Uncertain significance 44