| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | Schwannoma +3 more | GPathogenic/Likely pathogenic |
| | ADORA2A, C22orf15
+25 more | Copy number gain | Cerebellar ataxia | |
Click to view in NCBI Gene