MAP2K7 — 52 ClinVar variants

All ClinVar germline MAP2K7 variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 35 flagged for review →

9 Benign · 4 Likely benign · 39 Uncertain significance

Full MAP2K7 gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions

⚑ Evidence disagreements 35

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 23

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

All MAP2K7 variants

Benign 9

Likely benign 4

Uncertain significance 39