| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC130057927, LOC130057928
+1764 more | Copy number gain | See cases | |
| | LOC130057269, SNX22 (P16L) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | LOC130057269, SNX22 (R17T) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | LOC130057269, SNX22 (E21K) | Single nucleotide variant (missense variant +1 more) | not specified | |
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