ADAMTS7 — 368 ClinVar variants

All ClinVar germline ADAMTS7 variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 326 flagged for review →

2 Conflicting · 9 Benign · 1 Benign/Likely benign · 40 Likely benign · 316 Uncertain significance

Full ADAMTS7 gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions

⚑ Evidence disagreements 326

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 agree, ClinVar conflicts 1

ClinVar submitters conflict, but the independent predictors unanimously agree — a QC review flag, not a reclassification.

Predictors lean, ClinVar uncertain 169

ClinVar classifies these uncertain (VUS), but the independent predictors unanimously lean one way — a triage signal for review, not a reclassification. · showing the 150 best-reviewed of 169

Predictors split 156

The independent predictors disagree with each other — read with care. · showing the 150 best-reviewed of 156

All ADAMTS7 variants

Conflicting classifications of pathogenicity 2

Benign 9

Benign/Likely benign 1

Likely benign 40

Uncertain significance 316

Showing the top 300 by review status; the full set is in the sitemap.