GCOM1 — 100 ClinVar variants

All ClinVar germline GCOM1 variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 92 flagged for review →

5 Likely benign · 95 Uncertain significance

Full GCOM1 gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions

⚑ Evidence disagreements 92

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 76

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

All GCOM1 variants

Likely benign 5

  • p.Ala511= Single submitter Inborn genetic diseases
  • p.Arg523Gln Single submitter Inborn genetic diseases
  • p.Gly451Glu Single submitter Inborn genetic diseases
  • p.Ile454Val Single submitter Inborn genetic diseases
  • p.Lys508= Single submitter Inborn genetic diseases

Uncertain significance 95