| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LAYN, LOC126861337 (T53K +3 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LAYN, LOC126861337 (A66T +3 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene