| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | ARRB2, LOC126862469 (N24S +3 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | ARRB2, LOC132090475 (R169Q +2 more) | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | ARRB2, LOC126862469 (R283W +3 more) | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | ARRB2, LOC126862469 (Q57H +3 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (synonymous variant +2 more) | not provided | |
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