ADAMTS15 — 174 ClinVar variants

All ClinVar germline ADAMTS15 variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 156 flagged for review →

3 Pathogenic · 2 Likely pathogenic · 4 Benign · 1 Benign/Likely benign · 9 Likely benign · 155 Uncertain significance

Full ADAMTS15 gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions

⚑ Evidence disagreements 156

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 70

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

All ADAMTS15 variants

Pathogenic 3

  • c.1903-2A>G No assertion criteria arthrogryposis, distal, type 12
  • p.Gly761Ser No assertion criteria arthrogryposis, distal, type 12
  • p.Tyr41Ter No assertion criteria arthrogryposis, distal, type 12

Likely pathogenic 2

  • c.1903-2A>C Single submitter arthrogryposis, distal, type 12
  • p.Cys905Trp Single submitter arthrogryposis, distal, type 12

Benign 4

Benign/Likely benign 1

Likely benign 9

Uncertain significance 155