| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC126807556, SPARC (D274E +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | |
| | LOC126807556, SPARC (P253L +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126807556, SPARC (E251K +1 more) | Single nucleotide variant (missense variant) | not provided +2 more | |
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