EML6 — 337 ClinVar variants

All ClinVar germline EML6 variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 322 flagged for review →

1 Likely pathogenic · 5 Benign · 8 Likely benign · 323 Uncertain significance

Full EML6 gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions

⚑ Evidence disagreements 322

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 193

ClinVar classifies these uncertain (VUS), but the independent predictors unanimously lean one way — a triage signal for review, not a reclassification. · showing the 150 best-reviewed of 193

Predictors split 129

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

All EML6 variants

Likely pathogenic 1

Benign 5

Likely benign 8

Uncertain significance 323

Showing the top 300 by review status; the full set is in the sitemap.