| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (intron variant) | not specified +4 more | GConflicting classifications of pathogenicity |
| | RELN, SLC26A5-AS1 (T2885I) | Single nucleotide variant (missense variant) | Norman-Roberts syndrome | |
Click to view in NCBI Gene