| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | IFNGR2, LOC119266102 (L13F) | Single nucleotide variant (missense variant) | not provided +3 more | GConflicting classifications of pathogenicity |
| | IFNGR2, LOC119266102 (P23A) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
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