| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC129934738, SAP130 (P7S) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | LOC129934738, SAP130 (G19R) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | LOC129934738, SAP130 (A14G) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | LOC129934738, SAP130 (P3L) | Single nucleotide variant (missense variant +1 more) | not specified | |
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