| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC126860130, RELN
+1 more | Single nucleotide variant (splice acceptor variant) | Familial temporal lobe epilepsy 7 | |
| | RELN, SLC26A5-AS1 (I2754fs) | Deletion (frameshift variant) | Familial temporal lobe epilepsy 7 | |
| | | Single nucleotide variant (missense variant) | Familial temporal lobe epilepsy 7 | |
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