| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | RELN, SLC26A5-AS1 (R3429H +1 more) | Single nucleotide variant (missense variant) | Familial temporal lobe epilepsy 7 +1 more | |
| | RELN, SLC26A5-AS1 (K3100del) | Microsatellite (inframe_deletion) | Familial temporal lobe epilepsy 7 +6 more | GConflicting classifications of pathogenicity |
Click to view in NCBI Gene