CLDN34 — 27 ClinVar variants

All ClinVar germline CLDN34 variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 24 flagged for review →

4 Likely benign · 23 Uncertain significance

Full CLDN34 gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions

⚑ Evidence disagreements 24

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 CLDN34 variants

Likely benign 4

Uncertain significance 23