| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | OR52A1, LOC110011217 (P287A) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | OR52A1, LOC110011217 (A258T) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | OR52A1, LOC110011217 (C249Y) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC110011217, OR52A1 (A246S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC110011217, OR52A1 (L203M) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC110011217, OR52A1 (L190V) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC110011217, OR52A1 (T174K) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC110011217, OR52A1 (R168W) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC110011217, OR52A1 (I86V) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC110011217, OR52A1 (L68P) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC110011217, OR52A1 (E59K) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC110011217, OR52A1 (S24F) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
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