| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | | Single nucleotide variant (missense variant +1 more) | 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 +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | FBXO22, FBXO22-AS1 (E294K) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | FBXO22-AS1, FBXO22 (A311V) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | FBXO22, FBXO22-AS1 (A336T) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | FBXO22, FBXO22-AS1 (F348C) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
Click to view in NCBI Gene