| | | Single nucleotide variant (intron variant +1 more) | RELN-related disorder | |
| | RELN, SLC26A5-AS1 (R3387K) | Single nucleotide variant (missense variant) | RELN-related disorder +1 more | |
| | | Single nucleotide variant (synonymous variant) | RELN-related disorder +2 more | |
| | | Single nucleotide variant (synonymous variant) | RELN-related disorder +2 more | |
| | | Single nucleotide variant (synonymous variant) | Norman-Roberts syndrome +3 more | |
| | | Single nucleotide variant (synonymous variant) | RELN-related disorder +4 more | GConflicting classifications of pathogenicity |
| | LOC126860130, RELN +1 more (E3251K) | Single nucleotide variant (missense variant) | RELN-related disorder +2 more | |
| | | Deletion (intron variant) | RELN-related disorder +4 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +4 more | |
| | RELN, SLC26A5-AS1 (K3100del) | Microsatellite (inframe_deletion) | Norman-Roberts syndrome +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | RELN-related disorder | |
| | | Microsatellite (intron variant) | RELN-related disorder +2 more | |
| | SLC26A5-AS1, RELN (R2955C) | Single nucleotide variant (missense variant) | Norman-Roberts syndrome +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Familial temporal lobe epilepsy 7 +2 more | |
| | | Single nucleotide variant (intron variant) | RELN-related disorder | |
| | | Deletion (intron variant) | RELN-related disorder +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | RELN-related disorder +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | not provided +3 more | GConflicting classifications of pathogenicity |
| | | Deletion (intron variant) | RELN-related disorder | |
| | | Deletion (intron variant) | RELN-related disorder | |
| | | Single nucleotide variant (intron variant) | Norman-Roberts syndrome +4 more | |
| | | Single nucleotide variant (missense variant) | RELN-related disorder | |
| | | Single nucleotide variant (synonymous variant) | Norman-Roberts syndrome +2 more | |
| | | Single nucleotide variant (missense variant) | Norman-Roberts syndrome +2 more | |
| | | Single nucleotide variant (synonymous variant) | RELN-related disorder +2 more | |
| | | Single nucleotide variant (missense variant) | Norman-Roberts syndrome +2 more | |
| | | Single nucleotide variant (missense variant) | Norman-Roberts syndrome +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not specified +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | RELN-related disorder | |
| | | Single nucleotide variant (missense variant) | Norman-Roberts syndrome +2 more | |
| | | Single nucleotide variant (intron variant) | not specified +3 more | |
| | | Single nucleotide variant (intron variant) | RELN-related disorder | |
| | | Single nucleotide variant (intron variant) | RELN-related disorder | |
| | | Deletion (intron variant) | RELN-related disorder | |
| | | Single nucleotide variant (missense variant) | not provided +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | RELN-related disorder +2 more | |
| | | Single nucleotide variant (missense variant) | Norman-Roberts syndrome +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | not provided +3 more | |
| | | Single nucleotide variant (missense variant) | Familial temporal lobe epilepsy 7 +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Norman-Roberts syndrome +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | RELN-related disorder | |
| | | Single nucleotide variant (missense variant) | RELN-related disorder | |
| | | Single nucleotide variant (synonymous variant) | not specified +4 more | |
| | | Single nucleotide variant (synonymous variant) | Norman-Roberts syndrome +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Norman-Roberts syndrome +4 more | |
| | | Single nucleotide variant (missense variant) | RELN-related disorder +2 more | |
| | | Single nucleotide variant (synonymous variant) | RELN-related disorder | |
| | | Single nucleotide variant (synonymous variant) | RELN-related disorder +2 more | |
| | | Single nucleotide variant (missense variant) | Norman-Roberts syndrome +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Norman-Roberts syndrome +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | RELN-related disorder +2 more | |
| | | Deletion (intron variant) | RELN-related disorder +1 more | |
| | | Insertion (intron variant) | RELN-related disorder | |
| | | Single nucleotide variant (intron variant) | RELN-related disorder | |
| | | Single nucleotide variant (missense variant) | Norman-Roberts syndrome +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | RELN-related disorder +2 more | |
| | | Single nucleotide variant (missense variant) | RELN-related disorder +3 more | |
| | | Single nucleotide variant (synonymous variant) | Norman-Roberts syndrome +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | not provided +4 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +3 more | |
| | | Single nucleotide variant (missense variant) | RELN-related disorder | |
| | | Single nucleotide variant (missense variant) | not provided +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | not provided +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | RELN-related disorder +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | RELN-related disorder +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +4 more | |
| | | Single nucleotide variant (synonymous variant) | RELN-related disorder | |
| | | Inversion (missense variant) | Norman-Roberts syndrome +2 more | |
| | | Single nucleotide variant (missense variant) | RELN-related disorder +4 more | |
| | | Single nucleotide variant (intron variant) | RELN-related disorder | |
| | | Single nucleotide variant (missense variant) | RELN-related disorder | |
| | | Single nucleotide variant (intron variant) | not provided +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Norman-Roberts syndrome +5 more | |
| | | Single nucleotide variant (missense variant) | RELN-related disorder | |
| | | Single nucleotide variant (missense variant) | RELN-related disorder | |
| | | Single nucleotide variant (synonymous variant) | Familial temporal lobe epilepsy 7 +3 more | |
| | | Single nucleotide variant (intron variant) | RELN-related disorder +2 more | |
| | | Single nucleotide variant (synonymous variant) | RELN-related disorder +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | RELN-related disorder +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Norman-Roberts syndrome +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | RELN-related disorder | |
| | | Single nucleotide variant (missense variant) | RELN-related disorder | |
| | | Single nucleotide variant (missense variant) | Familial temporal lobe epilepsy 7 +2 more | GConflicting classifications of pathogenicity |
| | LOC126860131, RELN (M466I) | Single nucleotide variant (missense variant) | RELN-related disorder | |
| | | Single nucleotide variant (missense variant) | not specified +4 more | |
| | | Single nucleotide variant (missense variant) | RELN-related disorder +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Familial temporal lobe epilepsy 7 +2 more | |
| | | Single nucleotide variant (synonymous variant) | not specified +3 more | |
| | | Single nucleotide variant (missense variant) | not specified +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | RELN-related disorder | |
| | | Single nucleotide variant (intron variant) | not provided +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | RELN-related disorder +2 more | |
| | | Single nucleotide variant (missense variant) | RELN-related disorder | |
| | | Single nucleotide variant (missense variant) | not specified +4 more | GConflicting classifications of pathogenicity |
| | | Microsatellite (inframe_insertion) | RELN-related disorder +2 more | GConflicting classifications of pathogenicity |
| | | Microsatellite (inframe_insertion) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Microsatellite (inframe_insertion) | not specified +3 more | GConflicting classifications of pathogenicity |
| | | Microsatellite (inframe_insertion) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Microsatellite (5 prime UTR variant) | not provided +2 more | GConflicting classifications of pathogenicity |