APOH — 38 ClinVar variants

All ClinVar germline APOH variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 29 flagged for review →

1 Likely pathogenic · 9 Benign · 1 Likely benign · 27 Uncertain significance

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

⚑ Evidence disagreements 29

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 vs ClinVar 1

ClinVar calls these pathogenic, but the computational predictors lean tolerated — the highest-value review flag.

All APOH variants

Likely pathogenic 1

Benign 9

Likely benign 1

Uncertain significance 27