| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC129995965, SOX4 (S266G) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC129995965, SOX4 (A274V) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC129995965, SOX4 (A289V) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene