P2RY2 — 75 ClinVar variants

All ClinVar germline P2RY2 variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 68 flagged for review →

1 Benign · 5 Likely benign · 69 Uncertain significance

Full P2RY2 gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions

⚑ Evidence disagreements 68

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 57

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

All P2RY2 variants

Benign 1

Likely benign 5

Uncertain significance 69