| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC129930865, SYDE2 (M79I) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC129930865, SYDE2 (A26T) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC129930865, SYDE2 (S34F) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC129930865, SYDE2 (G47E) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
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