| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | HYOU1, LOC130006884 (V437L) | Single nucleotide variant (missense variant) | not specified | |
| | HYOU1, LOC130006884 (A429G) | Single nucleotide variant (missense variant) | not specified | |
| | HYOU1, LOC130006884 (A425V) | Single nucleotide variant (missense variant) | not provided +1 more | |
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