CCP110 — 140 ClinVar variants

All ClinVar germline CCP110 variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 121 flagged for review →

2 Likely pathogenic · 9 Benign · 8 Likely benign · 121 Uncertain significance

Full CCP110 gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions

⚑ Evidence disagreements 121

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 86

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

Predictors split 35

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

All CCP110 variants

Likely pathogenic 2

Benign 9

Likely benign 8

Uncertain significance 121