| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC130060786, LOC130060787
+633 more | Copy number gain | See cases | |
| | LOC130060889, STAT3 (T164N +2 more) | Single nucleotide variant (missense variant) | not provided | |
| | LOC130060889, STAT3 (S194L) | Single nucleotide variant (missense variant) | not provided +2 more | GConflicting classifications of pathogenicity |
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