| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC126862035, SYNE3 (W754G) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126862035, SYNE3 (V725M) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126862035, SYNE3 (K765Q) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126862035, SYNE3 (Q727P) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126862035, SYNE3 (A734S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126862035, SYNE3 (R790H) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene