CHP2 — 41 ClinVar variants

All ClinVar germline CHP2 variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 40 flagged for review →

1 Likely benign · 40 Uncertain significance

Full CHP2 gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions

⚑ Evidence disagreements 40

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 25

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

All CHP2 variants

Likely benign 1

Uncertain significance 40