| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | | Single nucleotide variant (intron variant) | Norman-Roberts syndrome +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | not specified +4 more | GConflicting classifications of pathogenicity |
| | RELN, SLC26A5-AS1 (C2732F) | Single nucleotide variant (missense variant) | Familial temporal lobe epilepsy 7 +1 more | |
Click to view in NCBI Gene