| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126860525, OC90 (H430P) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126860525, OC90 (S428T) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126860525, OC90 (S428G) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126860525, OC90 (A424D) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126860525, OC90 (P422L) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126860525, OC90 (A404S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | OC90, LOC126860525 (L389F) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |