| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Deletion | Agammaglobulinemia 8b, autosomal recessive | |
| | | Single nucleotide variant (intron variant) | Agammaglobulinemia 8, autosomal dominant | |
| | | Single nucleotide variant (missense variant) | not provided | |
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