| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC130059746, SNAI3 +1 more (R25T) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC130059746, SNAI3 +1 more (Q24E) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC130059746, SNAI3 +1 more (R14S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | SNAI3, LOC130059746 +1 more (H13R) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC130059746, SNAI3 +1 more (V7L) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene