ADRB1 — 80 ClinVar variants

All ClinVar germline ADRB1 variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 55 flagged for review →

1 Pathogenic · 8 Benign · 1 Benign/Likely benign · 13 Likely benign · 57 Uncertain significance

Full ADRB1 gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions

⚑ Evidence disagreements 55

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 vs ClinVar 1

ClinVar calls these pathogenic, but the computational predictors lean tolerated — the highest-value review flag.

Predictors lean, ClinVar uncertain 47

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

All ADRB1 variants

Pathogenic 1

  • p.Ala187Val No assertion criteria SHORT SLEEP, FAMILIAL NATURAL, 2 ⚠

Benign 8

Benign/Likely benign 1

Likely benign 13

Uncertain significance 57