| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC126862264, MEFV (I692del) | Deletion | Familial Mediterranean fever, autosomal dominant +3 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +6 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +3 more | |
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