| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC112081400, OR52B6 (H170Y) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC112081400, OR52B6 (L168M) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC112081400, OR52B6 (G108V) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
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