CHST7 — 42 ClinVar variants

All ClinVar germline CHST7 variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 37 flagged for review →

1 Conflicting · 2 Benign · 3 Likely benign · 36 Uncertain significance

Full CHST7 gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions

⚑ Evidence disagreements 37

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 CHST7 variants

Conflicting classifications of pathogenicity 1

Benign 2

Likely benign 3

Uncertain significance 36