| | | Single nucleotide variant (non-coding transcript variant +1 more) | MIF-related condition | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | MIF-related condition | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | MIF-related condition | |
| | ADORA2A, C22orf15 +25 more | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | not provided | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
| | | Copy number gain | Chromosome 22q11.2 microduplication syndrome | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
| | | Duplication | not provided | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | Unilateral renal agenesis | |
| | | Copy number gain | Chromosome 22q11.2 microduplication syndrome | |
| | | Deletion | Agammaglobulinemia 2, autosomal recessive | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | Generalized-onset seizure +1 more | |
| | ADORA2A, C22orf15 +25 more | Copy number gain | not provided | |
| | | Duplication | not provided | |
| | | Duplication | Epilepsy +1 more | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | Cat eye syndrome +1 more | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Deletion | not provided | |
| | | Duplication | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | not provided | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | not provided | |
| | | Copy number gain | not provided | |
| | ADORA2A, C22orf15 +25 more | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Duplication | not provided | |
| | | Copy number gain | 22q11.2 distal duplication syndrome | |
| | | Copy number gain | Global developmental delay | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number loss | not provided | |
| | | Copy number loss | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | not provided | |
| | | Duplication | Schizophrenia | |
| | | Duplication | Schizophrenia | |
| | | Duplication | Schizophrenia | |
| | ADORA2A, C22orf15 +25 more | Copy number gain | Cerebellar ataxia | |
| | ADORA2A, C22orf15 +25 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | ADORA2A, C22orf15 +25 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | C22orf15, C22orf23 +435 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number loss | Premature ovarian failure | |
| | | Copy number gain | See cases | |
| | ADORA2A, ADORA2A-AS1 +74 more | Copy number gain | See cases | |
| | ADORA2A, ADORA2A-AS1 +160 more | Copy number gain | See cases | |
| | ADORA2A, ADORA2A-AS1 +163 more | Copy number gain | See cases | |
| | ADORA2A, ADORA2A-AS1 +76 more | Copy number gain | See cases | |
| | ADORA2A, ADORA2A-AS1 +81 more | Copy number gain | See cases | |
| | LOC130067070, LOC130067071 +124 more | Copy number gain | See cases | |
| | ADORA2A, ADORA2A-AS1 +163 more | Copy number gain | See cases | |