STK38L — 38 ClinVar variants

All ClinVar germline STK38L variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 31 flagged for review →

2 Benign · 3 Likely benign · 33 Uncertain significance

Full STK38L gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions

⚑ Evidence disagreements 31

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 STK38L variants

Benign 2

  • p.Gly6= Multiple submitters
  • c.-7C>T No assertion criteria STK38L-related disorder

Likely benign 3

Uncertain significance 33