CYP4F8 — 57 ClinVar variants

All ClinVar germline CYP4F8 variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 55 flagged for review →

6 Likely benign · 51 Uncertain significance

Full CYP4F8 gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions

⚑ Evidence disagreements 55

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 split 40

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

All CYP4F8 variants

Likely benign 6

Uncertain significance 51