| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC129390449, OR8S1 (S193P) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC129390449, OR8S1 (N210H) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC129390449, OR8S1 (L213F) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC129390449, OR8S1 (I225F) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene