| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC126862917, STRN4 (V261L) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126862917, STRN4 (A248T) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene