GRIN2C — 180 ClinVar variants

All ClinVar germline GRIN2C variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 141 flagged for review →

6 Benign · 2 Benign/Likely benign · 18 Likely benign · 154 Uncertain significance

Full GRIN2C gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions

⚑ Evidence disagreements 141

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 113

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

Predictors split 28

The independent predictors disagree with each other — read with care.

All GRIN2C variants

Benign 6

Benign/Likely benign 2

Likely benign 18

Uncertain significance 154