MCHR2 — 45 ClinVar variants

All ClinVar germline MCHR2 variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 37 flagged for review →

2 Benign · 1 Likely benign · 42 Uncertain significance

Full MCHR2 gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions

⚑ Evidence disagreements 37

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 34

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

All MCHR2 variants

Benign 2

Likely benign 1

Uncertain significance 42