DOCK2 — 1198 ClinVar variants

All ClinVar germline DOCK2 variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 437 flagged for review →

18 Pathogenic · 16 Likely pathogenic · 15 Conflicting · 65 Benign · 12 Benign/Likely benign · 614 Likely benign · 458 Uncertain significance

Full DOCK2 gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions

⚑ Evidence disagreements 437

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 6

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

Predictors lean, ClinVar uncertain 225

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 225

Predictors split 206

The independent predictors disagree with each other — read with care. · showing the 150 best-reviewed of 206

All DOCK2 variants

Pathogenic 18

Likely pathogenic 16

Conflicting classifications of pathogenicity 15

Benign 65

Benign/Likely benign 12

Likely benign 614

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

Uncertain significance 458

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