| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | ATP2A2, LOC126861637 (P602L) | Single nucleotide variant (missense variant) | not provided | |
| | ATP2A2, LOC126861637 (A616V) | Single nucleotide variant (missense variant) | not provided | |
| | ATP2A2, LOC126861637 (P680L) | Single nucleotide variant (missense variant) | not provided | |
| | ATP2A2, LOC126861637 (I686fs) | Deletion (frameshift variant) | not provided | |
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