| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC126860791, SNAPC4 (S26L) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126860791, SNAPC4 (G24S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126860791, SNAPC4 (E16K) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene