| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC102724323, ALOX5 (S502I +4 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ALOX5, LOC102724323 (V619M +4 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ALOX5, LOC102724323 (R610G +4 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ALOX5, LOC102724323 (R522Q +4 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
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