| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | IRAK3, LOC130008234 (T15K) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | IRAK3, LOC130008235 (L32M) | Single nucleotide variant (missense variant) | not provided | |
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