PARD3 — 225 ClinVar variants

All ClinVar germline PARD3 variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 173 flagged for review →

2 Pathogenic · 1 Conflicting · 14 Benign · 1 Benign/Likely benign · 31 Likely benign · 176 Uncertain significance

Full PARD3 gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions

⚑ Evidence disagreements 173

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 vs ClinVar 1

ClinVar calls these pathogenic, but the computational predictors lean tolerated — the highest-value review flag.

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 128

ClinVar classifies these uncertain (VUS), but the independent predictors unanimously lean one way — a triage signal for review, not a reclassification.

Predictors split 43

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

All PARD3 variants

Pathogenic 2

Conflicting classifications of pathogenicity 1

Benign 14

Benign/Likely benign 1

Likely benign 31

Uncertain significance 176