GRM8 — 145 ClinVar variants

All ClinVar germline GRM8 variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 104 flagged for review →

1 Conflicting · 14 Benign · 22 Likely benign · 108 Uncertain significance

Full GRM8 gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions

⚑ Evidence disagreements 104

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 82

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

All GRM8 variants

Conflicting classifications of pathogenicity 1

Benign 14

Likely benign 22

Uncertain significance 108