| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant +1 more) | Epilepsy, familial adult myoclonic, 5 | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Epilepsy, familial adult myoclonic, 5 | |
| | CNTN2, LOC126805985 (P995S) | Single nucleotide variant (missense variant +1 more) | Epilepsy, familial adult myoclonic, 5 | |
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