| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC126860130, RELN
+1 more (Q3254H) | Single nucleotide variant (missense variant) | Seizure | |
| | RELN, SLC26A5-AS1 (K3100del) | Microsatellite (inframe_deletion) | Familial temporal lobe epilepsy 7 +6 more | GConflicting classifications of pathogenicity |
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