CLDN4 — 27 ClinVar variants

All ClinVar germline CLDN4 variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 25 flagged for review →

2 Likely benign · 25 Uncertain significance

Full CLDN4 gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions

⚑ Evidence disagreements 25

Variants where the independent computational evidence doesn't line up with the clinical picture — a QC signal for a second look, not a reclassification.

All CLDN4 variants

Likely benign 2

Uncertain significance 25