| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | RORA, RORA-AS1 (E362D +3 more) | Single nucleotide variant (missense variant) | Intellectual developmental disorder with or without epilepsy or cerebellar ataxia | |
| | RORA, RORA-AS1 (F349L +3 more) | Single nucleotide variant (missense variant) | Intellectual developmental disorder with or without epilepsy or cerebellar ataxia | |
| | | Single nucleotide variant (intron variant) | Intellectual developmental disorder with or without epilepsy or cerebellar ataxia | |
| | | Single nucleotide variant (missense variant +2 more) | Intellectual developmental disorder with or without epilepsy or cerebellar ataxia | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | |
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