LCP2 — 104 ClinVar variants

All ClinVar germline LCP2 variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 69 flagged for review →

1 Pathogenic · 16 Benign · 1 Benign/Likely benign · 16 Likely benign · 70 Uncertain significance

Full LCP2 gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions

⚑ Evidence disagreements 69

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 LCP2 variants

Pathogenic 1

  • c.957+1G>A No assertion criteria immunodeficiency 81

Benign 16

Benign/Likely benign 1

Likely benign 16

Uncertain significance 70