| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC130061806, SYNGR2 (A9G) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC130061806, SYNGR2 (A30T) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC130061806, SYNGR2 (A30S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene