| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (synonymous variant) | not provided +1 more | |
| | LOC129995011, SYNPO (P796L) | Single nucleotide variant (missense variant) | not specified +1 more | GConflicting classifications of pathogenicity |
| | LOC129995011, SYNPO (P799S) | Single nucleotide variant (missense variant) | not specified | |
| | LOC129995011, SYNPO (R801L) | Single nucleotide variant (missense variant) | not specified | |
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