| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC126860131, RELN (V479L) | Single nucleotide variant (missense variant) | Inborn genetic diseases +3 more | |
| | LOC126860131, RELN (T469P) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126860131, RELN (T468P) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126860131, RELN (D467A) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126860131, RELN (K460T) | Single nucleotide variant (missense variant) | Norman-Roberts syndrome +3 more | GConflicting classifications of pathogenicity |
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