PHRF1 — 412 ClinVar variants

All ClinVar germline PHRF1 variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 338 flagged for review →

1 Conflicting · 4 Benign · 56 Likely benign · 351 Uncertain significance

Full PHRF1 gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions

⚑ Evidence disagreements 338

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 315

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 315

All PHRF1 variants

Conflicting classifications of pathogenicity 1

Benign 4

Likely benign 56

Uncertain significance 351

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