S1PR4 — 33 ClinVar variants

All ClinVar germline S1PR4 variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 27 flagged for review →

1 Benign/Likely benign · 3 Likely benign · 29 Uncertain significance

Full S1PR4 gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions

⚑ Evidence disagreements 27

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 23

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

All S1PR4 variants

Benign/Likely benign 1

Likely benign 3

Uncertain significance 29