PRLR — 86 ClinVar variants

All ClinVar germline PRLR variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 67 flagged for review →

3 Pathogenic · 1 Likely pathogenic · 1 Conflicting · 3 Benign · 12 Likely benign · 66 Uncertain significance

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

⚑ Evidence disagreements 67

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 57

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

All PRLR variants

Pathogenic 3

  • p.Arg171Ter No assertion criteria familial hyperprolactinemia
  • p.His212Arg No assertion criteria familial hyperprolactinemia ⚠
  • p.Pro269Leu No assertion criteria familial hyperprolactinemia

Likely pathogenic 1

Conflicting classifications of pathogenicity 1

Benign 3

Likely benign 12

Uncertain significance 66