| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | DOCK8, LOC126860552 (D63N) | Single nucleotide variant (5 prime UTR variant +1 more) | Autosomal recessive hyper-IgE syndrome +2 more | |
| | DOCK8, LOC126860552 (P97T +1 more) | Single nucleotide variant (missense variant) | Autosomal recessive hyper-IgE syndrome +3 more | |
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