| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Copy number gain | See cases | |
| | LOC130058478, SOCS1 (R193C) | Single nucleotide variant (missense variant) | not provided | |
| | | Microsatellite (inframe_deletion) | not provided | |
| | LOC130058479, SOCS1 (A37fs) | Deletion (frameshift variant) | not provided | |
| | | Copy number gain | See cases | |
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